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LSHCHGJS001
06/29/2017
10:00 AM PST | 01:00 PM EST
Duration 60 mins
Gregory J Simms  
How To Bill Medicare for Durable Medical Equipment and Stay Legal Compliant

Learn that treating your Medicare patients with Durable Medical Equipment can be great for patient clinical outcomes, a great revenue stream and can be legally compliant. It will also lower healthcare costs. However one must know how to get the proper licensure and know the Federal & State Guidelines. This webinar will walk you through the process of how to do the....

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$165 
Single Attendee
(Only for one Participant)
$335 
Multiple Attendee
( 2 - 5 Participants)
$670 
Corporate Attendee
( 6 - 10 Participants)
$193 
  Recorded
(6 months unlimited access)
LSHCJLF001
06/29/2017
12:30 PM PST | 03:30 PM EST
Duration 90 mins
Janette Levey Frisch  
Employee Wellness Plans

In this webinar we will discuss what an Employee Wellness Program is, the different types of Wellness Programs and the different laws and regulations that come into play. While we will discuss the EEOC's new rules under the ADA and GINA, we will also look at HIPAA requirements, as well as ACA, Title VII and interplay with workers comp and workplace safety issues, and ....

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$165 
Single Attendee
(Only for one Participant)
$335 
Multiple Attendee
( 2 - 5 Participants)
$670 
Corporate Attendee
( 6 - 10 Participants)
$193 
  Recorded
(6 months unlimited access)
HIPBLT005
06/29/2017
10.00 AM PST | 01.00 PM EST
Duration 90 mins
Brian L Tuttle  
HIPAA for Dummies (HIPAA Boot Camp)

This lesson is going to get back to the basics using multiple real life scenarios and "what if's". My goal is to make this very confusing and not well explained law easy to understand for the typical staff member. I will uncover myths versus reality as it relates to this enigmatic law based on over 1000 risk assessments performed as well as years of experience in de....

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$165 
Single Attendee
(Only for one Participant)
$335 
Multiple Attendee
( 2 - 5 Participants)
$670 
Corporate Attendee
( 6 - 10 Participants)
$193 
  Recorded
(6 months unlimited access)
LSHCRD001
06/30/2017
10:00 AM PST | 01:00 PM EST
Duration 60 mins
Rachelle DSouza  
Use of Electronic Health Record Data (EHR) in FDA-regulated clinical investigations

This webinar will discuss FDA's current recommendations on using electronic health records in prospective clinical investigations of human drugs, biologics, medical devices and combination products.

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$165 
Single Attendee
(Only for one Participant)
$335 
Multiple Attendee
( 2 - 5 Participants)
$670 
Corporate Attendee
( 6 - 10 Participants)
$193 
  Recorded
(6 months unlimited access)
LSHCMRB003
07/03/2017
10:00 AM PST | 01:00 PM EST
Duration 60 mins
Mark R. Brengelman  
Beyond HIPAA: Patient Medical Records and Client Confidentiality in Mental Health

State law and contractual requirements mandate medical record keeping compliance. Then, compliance with HIPAA for protected health information in those records intersects with state laws and codes of ethics which mandate confidentiality, but there are many state law exceptions recognized by HIPAA. The exceptions sometimes allow and sometimes mandate what would otherwi....

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$165 
Single Attendee
(Only for one Participant)
$335 
Multiple Attendee
( 2 - 5 Participants)
$670 
Corporate Attendee
( 6 - 10 Participants)
$193 
  Recorded
(6 months unlimited access)
LSHCMBI003
07/03/2017
10:00 AM PST | 01:00 PM EST
Duration 60 mins
Michael Brodsky  
ISO/ IEC 17025:2017 Update: Everything Old is New Again

Many laboratories have successfully developed and implementing a functional quality management system that not only complies with the management and technical requirements of ISO/IEC 17025:2005 but also meets their needs. Some are still struggling to get accredited and even those already accredited still have issues as evidenced by the number of non-conformances cited....

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$165 
Single Attendee
(Only for one Participant)
$335 
Multiple Attendee
( 2 - 5 Participants)
$670 
Corporate Attendee
( 6 - 10 Participants)
$193 
  Recorded
(6 months unlimited access)
LSHCPJK003
07/05/2017
12:30 PM PST | 03:30 PM EST
Duration 60 mins
Jeff Kasoff  
Personnel Training to Assure QSR and ISO Compliance

Companies must assure their products are safe and effective for their intended use. To accomplish this, many companies have full teams of Design, Manufacturing, and Quality engineers responsible for implementing validated processes which utilize qualified components.
An equally critical requirement to provide assurance that products are safe and effective, to whic....

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$165 
Single Attendee
(Only for one Participant)
$335 
Multiple Attendee
( 2 - 5 Participants)
$670 
Corporate Attendee
( 6 - 10 Participants)
$193 
  Recorded
(6 months unlimited access)
LHSCDRD001
07/06/2017
10:00 AM PST | 01:00 PM EST
Duration 60 mins
David R Dills  
Medical Devices: Developing Effective Post Market Surveillance and Complaint Handling Systems

The session will provide an understanding and overview of GCP requirements and clinical quality assurance in detecting fraud and misconduct in clinical trials. Gain experience and learn more about detecting, correcting, and preventing clinical study misconduct and fraud at domestic and international clinical sites. The issue of fraud is again a focus within the clinic....

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$165 
Single Attendee
(Only for one Participant)
$335 
Multiple Attendee
( 2 - 5 Participants)
$670 
Corporate Attendee
( 6 - 10 Participants)
$193 
  Recorded
(6 months unlimited access)
HIPBLT003
07/07/2017
12.30 PM PST | 03.30 PM EST
Duration 60 mins
Brian L Tuttle  
Preparing for Imminent Federal HIPAA Audits.

This webinar will be addressing how practice/business managers (or compliance offers) need to get their HIPAA house in order before the imminent audits occur. It will also address major changes under the Omnibus Rule and any other applicable updates for 2017. Areas also covered will be texting, email, encryption, medical messaging, voice data and risk factors as ....

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$165 
Single Attendee
(Only for one Participant)
$335 
Multiple Attendee
( 2 - 5 Participants)
$670 
Corporate Attendee
( 6 - 10 Participants)
$193 
  Recorded
(6 months unlimited access)
LSHCSJM003
07/10/2017
10:00 AM PST | 01:00 PM EST
Duration 90 mins
Jose Mora  
Supplier Quality Management Utilizing Principles of Lean Documents and Lean Configuration

All life science businesses are required to maintain their Quality Management System (QMS) processes in a state of control, via controlled documents and objective evidence in the form of records. 
Utilizing suppliers as an extension of an organization's design and manufacturing capabilities presents unique challenges.

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$165 
Single Attendee
(Only for one Participant)
$335 
Multiple Attendee
( 2 - 5 Participants)
$670 
Corporate Attendee
( 6 - 10 Participants)
$193 
  Recorded
(6 months unlimited access)
LSHCMRB004
07/10/2017
10:00 AM PST | 01:00 PM EST
Duration 60 mins
Mark R. Brengelman  
Case Study: A Step-by-Step Analysis of the Most Salacious Sexual Misconduct Case Between Doctor and Patient

Learn to identify, understand, and defend against sexual misconduct cases in the health care profession with an in-depth analysis of the most salacious sexual misconduct case between doctor and patient. These civil (and even criminal) investigations target health care practitioners who have engaged in romantic and sexual improprieties with the patient.

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$165 
Single Attendee
(Only for one Participant)
$335 
Multiple Attendee
( 2 - 5 Participants)
$670 
Corporate Attendee
( 6 - 10 Participants)
$193 
  Recorded
(6 months unlimited access)
LSHCGJS002
07/11/2017
10:00 AM PST | 01:00 PM EST
Duration 60 mins
Gregory J Simms  
Strategies for billing medicare for durable medical equipment -from getting DME PTAN# to full accreditation

Learn how to provide your Medicare patients with Durable Medical Equipment to maximize patient clinical outcomes while developing a great revenue stream. The key is how to be legally compliant. Understand the process in how to get the proper licensure called DME PAN # and know the Federal & State Guidelines. Then learn how to get fully Accredited that can grow you....

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$165 
Single Attendee
(Only for one Participant)
$335 
Multiple Attendee
( 2 - 5 Participants)
$670 
Corporate Attendee
( 6 - 10 Participants)
$193 
  Recorded
(6 months unlimited access)
LSHCHPH003
07/12/2017
10:00 AM PST | 01:00 PM EST
Duration 60 mins
Paul Hales  
HIPAA - 7 Deadly Sins - 7 Simple Solutions

Top 7 HIPAA Violation Concerns revealed by Federal HIPAA Compliance Audits ordered by Congress. The U. S. Department of Health and Human Services (HHS) is conducting mandatory HIPAA Compliance Audits of covered entities and business associates to ensure they comply with HIPAA Privacy and Security Law. HHS's HIPAA Compliance Audit has more than 170 detailed sections - ....

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$165 
Single Attendee
(Only for one Participant)
$335 
Multiple Attendee
( 2 - 5 Participants)
$670 
Corporate Attendee
( 6 - 10 Participants)
$193 
  Recorded
(6 months unlimited access)
LSHCHEW003
07/12/2017
10:00 AM PST | 01:00 PM EST
Duration 60 mins
Edwin Waldbusser  
How to Conduct a Human Factors/ Usability Validation Test following ISO 62366 and the 2016 FDA Guidance

This webinar will explain the procedure described in ISO62366 and the 2016 FDA Guidance for a compliant human factors/ usability validation. HF/U validation is very different from device validation. For example, success criteria is qualitative rather than quantitative as is in device validation. Claiming success because eg. 95% of test participants did not commit a us....

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$165 
Single Attendee
(Only for one Participant)
$335 
Multiple Attendee
( 2 - 5 Participants)
$670 
Corporate Attendee
( 6 - 10 Participants)
$193 
  Recorded
(6 months unlimited access)
LSHCSCP003
07/13/2017
10:00 AM PST | 01:00 PM EST
Duration 60 mins
Carl Patterson  
Sterilization of Pharmaceutical Products and Medical Devices

This topic will discuss the methods of sterilization to be used on medical devices and pharmaceutical products. Understanding the regulations pertaining to sterilization of products will help to decide with method to use for your product. The advantages and disadvantages of each will be discussed. Validation of each sterilization method will be discussed and how best ....

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$165 
Single Attendee
(Only for one Participant)
$335 
Multiple Attendee
( 2 - 5 Participants)
$670 
Corporate Attendee
( 6 - 10 Participants)
$193 
  Recorded
(6 months unlimited access)
LSHCMRB005
07/17/2017
10:00 AM PST | 01:00 PM EST
Duration 60 mins
Mark R. Brengelman  
The Regulation of Emergency Medical Services - An Overview of Regulation by Focusing on One State's Model of Control, with an Extra Segment on Case Law Applying How EMS Laws Apply in the Real World to Everyday Citizens

Learn to identify, understand, and apply laws and regulations governing emergency medical services in the health care profession with an in-depth analysis of a state agency's regulation of these life-or-death medical services.

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$165 
Single Attendee
(Only for one Participant)
$335 
Multiple Attendee
( 2 - 5 Participants)
$670 
Corporate Attendee
( 6 - 10 Participants)
$193 
  Recorded
(6 months unlimited access)
LSHCLSH005
07/18/2017
10:00 AM PST | 01:00 PM EST
Duration 75 mins
Laura S. Hargraves  
Best Practices in Nursing Documentation: Writing Effective and Legal Proof Notes

This healthcare documentation webinar will discuss how to create a lawsuit-proof, auditable nursing documentation and how to maintain compliance over the course of the document life-time. You will learn how to de-risk your documentation so as to withstand legal scrutiny.

Documentation is the backbone of Medical Necessity and support for services provided. Understa....

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$165 
Single Attendee
(Only for one Participant)
$335 
Multiple Attendee
( 2 - 5 Participants)
$670 
Corporate Attendee
( 6 - 10 Participants)
$193 
  Recorded
(6 months unlimited access)
LSHCMRB001
07/19/2017
10:00 AM PST | 01:00 PM EST
Duration 60 mins
Mark R. Brengelman  
Health Care Investigations by the Government - How They Do It.

State government agencies tasked with investigating alleged misconduct in health care generally follow proscribed steps in investigating the misconduct. This can include agencies with authority over individually licensed health care practitioners or with authority over the administration of government health care programs - whose budgets are in the hundreds of million....

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$165 
Single Attendee
(Only for one Participant)
$335 
Multiple Attendee
( 2 - 5 Participants)
$670 
Corporate Attendee
( 6 - 10 Participants)
$193 
  Recorded
(6 months unlimited access)
LSHCHJ004
07/19/2017
10:00 AM PST | 01:00 PM EST
Duration 60 mins
Howard Jones  
The Requirements & Responsibilities of a HIPAA Security/Privacy Officer

Discussions, presentation, and webinars regarding HIPAA regulations are usually addressed from the perspective of what the regulations entail, the necessity of compliance with the regulations, and the consequences of willful neglect or non-compliance. 
This presentation addresses HIPAA regulations from a different perspective - from a personal perspective - fr....

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$165 
Single Attendee
(Only for one Participant)
$335 
Multiple Attendee
( 2 - 5 Participants)
$670 
Corporate Attendee
( 6 - 10 Participants)
$193 
  Recorded
(6 months unlimited access)
LHSCDRD002
07/20/2017
10.00 AM PST | 01.00 PM EST
Duration 60 mins
David R Dills  
GCP Audits - Best Practices for Ensuring Compliance & Detecting Fraud and Misconduct in Clinical Trials

An effective complaint handling system is an extremely important part of any quality system whether you are a medical device or pharmaceutical manufacturer. Manufacturers should understand that any complaint received on a product shall be evaluated and, if necessary, thoroughly investigated and analyzed, and corrective action shall be taken. Manufacturers must ensure ....

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$165 
Single Attendee
(Only for one Participant)
$335 
Multiple Attendee
( 2 - 5 Participants)
$670 
Corporate Attendee
( 6 - 10 Participants)
$193 
  Recorded
(6 months unlimited access)
LSHCJAT001
07/24/2017
10:00 AM PST | 01:00 PM EST
Duration 60 mins
Joseph Azary  
Transition to ISO 13485:2016

This course will provide an overview of the differences between the 2016 version of ISO 13485 compared to the existing version, and how to transition to the standard. 

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$165 
Single Attendee
(Only for one Participant)
$335 
Multiple Attendee
( 2 - 5 Participants)
$670 
Corporate Attendee
( 6 - 10 Participants)
$193 
  Recorded
(6 months unlimited access)
HIPBLT001
07/24/2017
10.00 AM PST | 01.00 PM EST
Duration 180 mins
Brian L Tuttle  
3-Hour Virtual Seminar on HIPAA Phase 2 Audits 2017 updates - an Insiders Perspective

I will be speaking to real life audits conducted by the Federal government for Phase 2 and beyond (I've been on both sides of these audits) what your highest risks are for being fined (some of the risk factors may surprise you). 
It seems almost daily I am receiving calls from nervous practice managers and compliance officers all over the USA regarding a HIPAA....

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$275 
Single Attendee
(Only for one Participant)
$555 
Multiple Attendee
( 2 - 5 Participants)
$1110 
Corporate Attendee
( 6 - 10 Participants)
$425 
  Recorded
(6 months unlimited access)
HIPBLT007
07/26/2017
12.30 PM PST | 03.30 PM EST
Duration 60 mins
Brian L Tuttle  
Understanding HIPAA Risks as a Medical Practice Manager

This lesson will be addressing how medical practice managers (or compliance offers) need to get their HIPAA house in order before the imminent audits occur. It will also address major changes under the Omnibus Rule and any other applicable updates for 2017.
There are an enormous amount of issues and risks for covered entities these days.
I will speak on sp....

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$165 
Single Attendee
(Only for one Participant)
$335 
Multiple Attendee
( 2 - 5 Participants)
$670 
Corporate Attendee
( 6 - 10 Participants)
$193 
  Recorded
(6 months unlimited access)
LSHCHJA023
07/26/2017
10:00 AM PST | 01:00 PM EST
Duration 60 mins
Jay Anstine  
HIPAA and The Front Office.

This presentation will provide strategies and insights targeted at the front office staff to proactively manage and maintain HIPAA compliance. More specifically, it will cover common front office violations, strategies for safeguarding protected health information ("PHI") and handling patient complaints. It will also highlight recent HIPAA enforcement trends.

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$165 
Single Attendee
(Only for one Participant)
$335 
Multiple Attendee
( 2 - 5 Participants)
$670 
Corporate Attendee
( 6 - 10 Participants)
$193 
  Recorded
(6 months unlimited access)
LSHCUJR001
07/31/2017
12.30 PM PST | 03.30 PM EST
Duration 90 mins
John Ryan  
Using Your Food Safety Data to Drive Cost Reductions and Process Improvements

In today's world of food safety, everyone in the supply chain is challenged to document what they are doing. This seemingly expensive documentation yields data that is valuable to cutting costs, improving food safety, meeting legal requirements and improving business processes.

But most companies do not yet know how to use the data they spend so much time and m....

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$165 
Single Attendee
(Only for one Participant)
$335 
Multiple Attendee
( 2 - 5 Participants)
$670 
Corporate Attendee
( 6 - 10 Participants)
$193 
  Recorded
(6 months unlimited access)
LSHCCJA016
08/09/2017
10:00 AM PST | 01:00 PM EST
Duration 60 mins
Jay Anstine  
Compliance with the CMS Physician Open Payments Rule.

Open Payments is a federal program under the Centers for Medicare and Medicaid Services ("CMS") that collects certain information relating to payments and other items of value provided to physicians from drug and device companies. Examples include: speaking fees, gifts, meals, and covering the cost of travel expenses to name a few. The Open Payments program also inc....

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$165 
Single Attendee
(Only for one Participant)
$335 
Multiple Attendee
( 2 - 5 Participants)
$670 
Corporate Attendee
( 6 - 10 Participants)
$193 
  Recorded
(6 months unlimited access)
HIPHSSK001
08/09/2017
10:00 AM PST | 01:00 PM EST
Duration 60 mins
Srini Kolathur  
HIPAA-HITECH assessment for Healthcare Business Associates - 2017

As the compliance deadline for new HIPAA-HITECH rule approaches, it becomes imperative for healthcare business associate organizations to develop strategies to protect electronic health information, and comply with HIPAA-HITECH regulations.
This instructor-led one-day training will teach you how to design, implement, and administer comprehensive healthcare IT compl....

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$165 
Single Attendee
(Only for one Participant)
$335 
Multiple Attendee
( 2 - 5 Participants)
$670 
Corporate Attendee
( 6 - 10 Participants)
$193 
  Recorded
(6 months unlimited access)
LSHCGRG002
08/10/2017
10:00 AM PST | 01:00 PM EST
Duration 60 mins
Roger Cowan  
GMP Environmental Monitoring for Pharmaceutical Clean Rooms

Environmental Monitoring looks at the end results of the Environmental Control program - the microbiological and particulate quality of the clean room.
As the FDA Guideline on Aseptic Processing GMP (2004) states:
"In aseptic processing, one of the most important laboratory controls is the environmental monitoring program. This program provides meaningful inf....

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$165 
Single Attendee
(Only for one Participant)
$335 
Multiple Attendee
( 2 - 5 Participants)
$670 
Corporate Attendee
( 6 - 10 Participants)
$193 
  Recorded
(6 months unlimited access)
HIPBLT006
08/15/2017
12.30 PM PST | 03.30 PM EST
Duration 60 mins
Brian L Tuttle  
HIPAA and the Business Associate

The objectives of this course will be to go over the specific risks associated with business associates as it relates to HIPAA compliance.
I will uncover myths versus reality as it relates to this very enigmatic law based on over 1000 risk assessments performed as well as years of experience in dealing directly with the Office of Civil Rights HIPAA auditors.

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$165 
Single Attendee
(Only for one Participant)
$335 
Multiple Attendee
( 2 - 5 Participants)
$670 
Corporate Attendee
( 6 - 10 Participants)
$193 
  Recorded
(6 months unlimited access)
LSHCNJA020
08/17/2017
10:00 AM PST | 01:00 PM EST
Duration 60 mins
Jay Anstine  
Navigating the Politics of Healthcare from the Compliance Role

This presentation will cover four main strategies the compliance professional can use to navigate the politics of healthcare to obtain buy-in to the compliance program. Additionally, the presentation will include strategies for improved communications with physicians and healthcare leaders.  

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$165 
Single Attendee
(Only for one Participant)
$335 
Multiple Attendee
( 2 - 5 Participants)
$670 
Corporate Attendee
( 6 - 10 Participants)
$193 
  Recorded
(6 months unlimited access)
LSHCIMBI004
08/21/2017
12:30 PM PST | 03:30 PM EST
Duration 60 mins
Michael Brodsky  
Is it Method Verification or Validation, or Just Semantics?

This Webinar will discuss the distinction between and requirements for method validation and method verification, to comply with ISO/IEC Standard 17025 for laboratory accreditation. Quantitative and Qualitative methods have different performance measurement requirements and require different statistical analyses. Although method validation and method verification are ....

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$165 
Single Attendee
(Only for one Participant)
$335 
Multiple Attendee
( 2 - 5 Participants)
$670 
Corporate Attendee
( 6 - 10 Participants)
$193 
  Recorded
(6 months unlimited access)
HIPHTS001
08/21/2017
12:30 AM PST | 03:30 PM EST
Duration 60 mins
Theresa K. Sheppard  
HIPAA: HIGHLIGHTS HOOPLA and HOOEY

Buying a fill-in- the-blank template does not equal HIPAA compliance, and doing nothing, or saying "I didn't know" can result in willful negligence. Translation: Fines that start at $10,000 and go up exponentially for each violation. I teach healthcare practices who want to be HIPAA compliant, but don't want the time consuming frustration or risk that comes with not k....

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$165 
Single Attendee
(Only for one Participant)
$335 
Multiple Attendee
( 2 - 5 Participants)
$670 
Corporate Attendee
( 6 - 10 Participants)
$193 
  Recorded
(6 months unlimited access)
LSHCWJL002
08/22/2017
10.00 AM PST | 01.00 PM EST
Duration 90 mins
Janette Levey Frisch  
What Employers Need to Know about Medical Marijuana In the Workplace

Most recent laws legalizing marijuana use have been geared towards removing criminal penalties for users, and do not fully address workplace issues posed by medical marijuana. Some state laws explicitly prohibit employers from discriminating against employees because of their status of medi....

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$165 
Single Attendee
(Only for one Participant)
$335 
Multiple Attendee
( 2 - 5 Participants)
$670 
Corporate Attendee
( 6 - 10 Participants)
$193 
  Recorded
(6 months unlimited access)
HIPHTSK002
08/23/2017
10:00 AM PST | 01:00 PM EST
Duration 60 mins
Srini Kolathur  
How to Manage OCR, HHS HIPAA and HITECH Audit

Among other things, the HITECH Act significantly strengthened HIPAA enforcement activities. In addition to increasing penalties, allowing enforcement by state attorneys general, requiring notices of breaches, and making business associates directly subject to penalties, the HITECH Act mandated that Office for Civil Rights of HHS conduct HIPAA audits. This one-hour web....

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$165 
Single Attendee
(Only for one Participant)
$335 
Multiple Attendee
( 2 - 5 Participants)
$670 
Corporate Attendee
( 6 - 10 Participants)
$193 
  Recorded
(6 months unlimited access)
LSHCBJA015
08/30/2017
10:00 AM PST | 01:00 PM EST
Duration 60 mins
Jay Anstine  
Breach Notification Rule: A Blueprint for Conducting Consistent Risk Assessments.

This presentation will provide a blueprint for consistently conducting risk assessments under the HIPAA Breach Notification Rule. More specifically, it will address topics such as what constitutes a breach, what to include in a Breach Notification policy, how to conduct a risk assessment analysing any issue, and how to document your risk assessment. This presentation....

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$165 
Single Attendee
(Only for one Participant)
$335 
Multiple Attendee
( 2 - 5 Participants)
$670 
Corporate Attendee
( 6 - 10 Participants)
$193 
  Recorded
(6 months unlimited access)
LSHCTMBI004
09/05/2017
12:30 PM PST | 03:30 PM EST
Duration 60 mins
Michael Brodsky  
The Revised Total Coliform Rule (RTCR)

Total coliforms are a group of related bacteria that are (with few exceptions) not harmful to humans, but are found in human waste (sewage). A variety of microbial pathogens in sewage can potentially cause health problems if humans ingest them. EPA no longer considers enumeration of total coliforms a useful indicator of other pathogens for drinking water. Total colifo....

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$165 
Single Attendee
(Only for one Participant)
$335 
Multiple Attendee
( 2 - 5 Participants)
$670 
Corporate Attendee
( 6 - 10 Participants)
$193 
  Recorded
(6 months unlimited access)
LSHCCJA017
09/08/2017
10:00 AM PST | 01:00 PM EST
Duration 60 mins
Jay Anstine  
Conducting Effective Compliance Investigation Interviews.

This presentation will give attendees a blueprint for conducting effective compliance investigation interviews.  Given that responding to detected offenses are included in the Seven Elements of an Effective Compliance Program as deemed by the Office of Inspector General ("OIG"), this webinar is intended to provide helpful str....

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$165 
Single Attendee
(Only for one Participant)
$335 
Multiple Attendee
( 2 - 5 Participants)
$670 
Corporate Attendee
( 6 - 10 Participants)
$193 
  Recorded
(6 months unlimited access)
HIPHHSK003
09/13/2017
10:00 AM PST | 01:00 PM EST
Duration 60 mins
Srini Kolathur  
HIPAA-HITECH Assessment of your Cloud Service Providers

The primary objective of this 60 minute webinar is to help organization identify the key vulnerabilities with cloud service providers by reviewing the best practices to evaluate, engage and monitor online service providers to protect ePHI handled on behalf of the Covered Entity.

  • Have you identified the e-PHI with your cloud service providers? This includes ....

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$165 
Single Attendee
(Only for one Participant)
$335 
Multiple Attendee
( 2 - 5 Participants)
$670 
Corporate Attendee
( 6 - 10 Participants)
$193 
  Recorded
(6 months unlimited access)
LHSCMJA014
09/15/2017
10.00 PM PST | 01.00 PM EST
Duration 60 mins
Jay Anstine  
Medical Director Contracting: Key Pitfalls to Avoid.

This webinar will discuss key compliance issues with respect to medical director contracts. More specifically, it will discuss the regulatory framework governing medical director contracts, key compliance issues, how to audit for medical director contract compliance, and recent government enforcement trends relating to medical director agreements.  

View Details

$165 
Single Attendee
(Only for one Participant)
$335 
Multiple Attendee
( 2 - 5 Participants)
$670 
Corporate Attendee
( 6 - 10 Participants)
$193 
  Recorded
(6 months unlimited access)
LSHCPJA018
09/28/2017
10:00 AM PST | 01:00 PM EST
Duration 60 mins
Jay Anstine  
Protecting Your Organization Against Sanctions for Ineffective Exclusion Screening.

Under certain circumstances (such as convictions for patient abuse and violations of the anti-kickback statute), the Department of Health and Human Services, Office of Inspector General ("OIG") is required to exclude persons from federal healthcare programs (e.g. Medicare, Medicaid). In other circumstances,(such as civil and criminal violations of healthcare laws), t....

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$165 
Single Attendee
(Only for one Participant)
$335 
Multiple Attendee
( 2 - 5 Participants)
$670 
Corporate Attendee
( 6 - 10 Participants)
$193 
  Recorded
(6 months unlimited access)
LSHCLJA013
10/11/2017
10.00 AM PST | 01.00 PM EST
Duration 60 mins
Jay Anstine  
Looking Inward: Assessing the Effectiveness of Your Compliance Program.

This webinar is designed to walk attendees through a self-assessment of the effectiveness of his/her compliance program to determine if the program is meeting the Federal government's standards (e.g. The Office of Inspector General's "Seven Elements of an Effective Compliance Program"). More specifically, this presentation will walk through a checklist of questions di....

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$165 
Single Attendee
(Only for one Participant)
$335 
Multiple Attendee
( 2 - 5 Participants)
$670 
Corporate Attendee
( 6 - 10 Participants)
$193 
  Recorded
(6 months unlimited access)
LSHCMEW004
10/24/2017
10:00 AM PST | 01:00 PM EST
Duration 60 mins
Edwin Waldbusser  
Mobile Medical Apps (Is It a FDA Regulated Device) and Cybersecurity

This webinar will explain how to determine if your app is a medical device and if it will be subject to FDA requirements. The FDA approval process for a new app will be explained including FDA requirements for software validation which are more extensive than just testing performance.
Cybersecurity is very important for mobile apps. The FDA requirements for cyberse....

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$165 
Single Attendee
(Only for one Participant)
$335 
Multiple Attendee
( 2 - 5 Participants)
$670 
Corporate Attendee
( 6 - 10 Participants)
$193 
  Recorded
(6 months unlimited access)
LSHCHJA019
10/27/2017
10:00 AM PST | 01:00 PM EST
Duration 60 mins
Jay Anstine  
Healthcare Fraud: Current Legislative and Regulatory Update.

This presentation will provide a general overview of the key legislative and regulatory developments in the area of healthcare fraud and abuse. For the key regulatory developments, Mr. Anstine will walk through notable cases to highlight key takeaways attendees should be aware of relative to help safeguard the operations of their own organizations.  

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$165 
Single Attendee
(Only for one Participant)
$335 
Multiple Attendee
( 2 - 5 Participants)
$670 
Corporate Attendee
( 6 - 10 Participants)
$193 
  Recorded
(6 months unlimited access)
LSHCTJA014
11/15/2017
12.30 PM PST | 03.30 PM EST
Duration 60 mins
Jay Anstine  
Tis the Season: Navigating the Compliance Challenges with Holiday Gifts

This webinar is designed to help attendees navigate through the compliance challenges related to holiday gift giving and receiving with physicians, vendors, patients, and co-workers. More specifically, it will discuss the regulatory framework surrounding gifts, common gifting scenarios, the pitfalls to avoid, and strategies for drafting organizational gift policies.

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$165 
Single Attendee
(Only for one Participant)
$335 
Multiple Attendee
( 2 - 5 Participants)
$670 
Corporate Attendee
( 6 - 10 Participants)
$193 
  Recorded
(6 months unlimited access)
LSHCUJA021
12/06/2017
10:00 AM PST | 01:00 PM EST
Duration 60 mins
Jay Anstine  
Understanding the Decision Points of Self-Disclosures and Repayment Obligations.

Historically, providers and suppliers enrolled in federal government healthcare programs have reconciled and returned overpayments through various post-payment audits. Additionally, these same entities have voluntarily returned self-identified overpayment through various self-disclosure methods made available to them. When Congress passed the Fraud Enforcement Recov....

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$165 
Single Attendee
(Only for one Participant)
$335 
Multiple Attendee
( 2 - 5 Participants)
$670 
Corporate Attendee
( 6 - 10 Participants)
$193 
  Recorded
(6 months unlimited access)
LSHCSJA022
12/13/2017
10:00 AM PST | 01:00 PM EST
Duration 60 mins
Jay Anstine  
Strategies for Becoming a Business Partner to Your Healthcare Leaders.

All too often compliance is seen as an obstacle or otherwise viewed negatively by healthcare leaders. This presentation will discuss strategies and insights to help the compliance officer position himself or herself to becoming a business partner to those in operations. Mr. Anstine will focus on several key strategies you can take to help change the perception of c....

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$165 
Single Attendee
(Only for one Participant)
$335 
Multiple Attendee
( 2 - 5 Participants)
$670 
Corporate Attendee
( 6 - 10 Participants)
$193 
  Recorded
(6 months unlimited access)
 
LSHCJA011
Duration 90 mins
View Anytime
Jay Anstine  
Monitoring and Investigating Drug Diversion

This webinar will walk attendees through monitoring against drug diversion and investigating alleged diversions. More specifically, it will discuss the warning signs of diversion, common methods used to carry out diversion, potential organizational vulnerabilities, investigating a diversion case from beginning to end, and offer tips for safeguarding against diversion....

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$193 Recorded (6 months unlimited access)
 
LSHCHEW002
Duration 60 mins
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Edwin Waldbusser  
Human Factors/ Usability following ISO 62366 and new FDA Guidance

Human Factors/ Usability is the analysis of how people interact with medical devices. The process of conducting rigorous human factors studies throughout the design process, integrating it with the device risk analysis and design process, and validating the effectiveness of the studies will....

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$193 Recorded (6 months unlimited access)
 
LSHCGCP002
Duration 60 mins
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Carl Patterson  
GMP Auditing for Pharmaceutical Manufacturing

Auditing involves a comprehensive review of vendors that will provide resources and/or services. The ICH Q10 document provides an outline on the pharmaceutical drug product life-cycle. Through the review of ICH Q8, Q9, and Q10, the participant will be able to audit the various activities associated with the different stages of the product lifecycle. By using a scien....

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$193 Recorded (6 months unlimited access)
 
LSHCIPH002
Duration 60 mins
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Paul Hales  
New HIPAA Rules for Communicating with Patients by Unencrypted Email and Text Messages

Communicating with patients by unencrypted email and text message (SMS) about a variety of topics (appointment reminders, patient satisfaction, etc.) is growing dramatically. The HIPAA Rules for sending Protected Health Information (PHI) by electronic messages have been clarified. But most Providers and Business Associates are not following the HIPAA Rules.
Email a....

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$193 Recorded (6 months unlimited access)
 
LSHCMRB002
Duration 60 mins
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Mark R. Brengelman  
Evidence-Based Dentistry - A New Standard for Disciplinary Actions.

Learn to identify, understand, and defend against new legal standards in dentistry that may apply to state licensure disciplinary actions and to civil claims for malpractice. Either claim may result in ruinous practice and career consequences for the health care professional held to an objective standard of care for dentists.
"Unprofessional conduct" and "negli....

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$193 Recorded (6 months unlimited access)
 
HIPBLT004
Duration 60 mins
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Brian L Tuttle  
HIPAA Audits - An Insiders Perspective

Speaker will be speaking to real life audits conducted by the Federal government for Phase 2 and beyond (He has been on both sides of these audits) what your highest risks are for being fined (some of the risk factors may surprise you). It seems almost daily I am receiving calls from nervous practice managers and compliance officers all over the USA regarding a HIPAA ....

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$193 Recorded (6 months unlimited access)
 
LSHCHJK004
Duration 60 mins
View Anytime
Jeff Kasoff  
How FDA Trains Its Investigators to Review CAPA, and Best Practices for Preparation

Year after year, CAPA is the subsystem cited most frequently during FDA inspections. During an inspection, FDA personnel will take a great deal of time reviewing your company's CAPA system. What will they look for? This session will discuss techniques used by the FDA to review your CAPA system. The documents used by FDA to train their inspectors to review yo....

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$193 Recorded (6 months unlimited access)
 
LSHCRD002
Duration 90 mins
View Anytime
Rachelle DSouza  
FDA Regulation, 3D Printing and Medical Devices

This webinar on 3D printing will cover FDA's expectations regarding the design, manufacture, testing and approval of 3D printed medical devices.

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$193 Recorded (6 months unlimited access)
 
LSHCAWMC002
Duration 120 mins
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William Mack Copeland  
Anti-Kickback, Fraud, Stark, and Marketing - Where are the Landmines?

This webinar will provide an in-depth understanding of the Federal False Claims Act, Federal Anti-Kickback and Stark laws, and discuss how marketing activities can trigger either or both.

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$193 Recorded (6 months unlimited access)
 
HIPBLT002
Duration 60 mins
View Anytime
Brian L Tuttle  
HIPAA and Personal Devices (myths vs realities)

This lesson will be going into great detail regarding you practice or business information technology and how it relates to the HIPAA Security Rule, in particular portable devices.
Areas covered will be texting, email, encryption, medical messaging, voice data and risk factors as they relate to personal devices.
I will uncover myths versus reality as it rela....

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$193 Recorded (6 months unlimited access)
 
LHSCTJA016
Duration 60 mins
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Jay Anstine  
Tracking Physician Gifts Under The Stark Non-Monetary Compensation Rule.

The Stark law generally prohibits physicians from referring Medicare patients for designated health services ("DHS") to an entity the physician or immediate family member has a financial relationship with, unless an exception applies. Under Stark, there is an exception known as the Non-Monetary Compensation ("NMC")exception (42 C.F.R. 411.357(k) that allows DHS entit....

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$193 Recorded (6 months unlimited access)
 
LSHCEW002
Duration 60 mins
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Edwin Waldbusser  
How to Prepare a FDA 510(k) submission

we will explain what a 510(k) is and the procedure to prepare the submission. the several types of 510(k) will be explained.Each part of the submission will be explained. The very confusing concepts of predicate device and substantial equivalence will be discussed. How to find an acceptable predicate device will be taught. FDA places special emphasis on device softwar....

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$193 Recorded (6 months unlimited access)
 
LSHCACP001
Duration 60 mins
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Carl Patterson  
Auditing for Microbiological Aspects of Pharmaceutical and Biopharmaceutical Manufacturing

The seminar provides a comprehensive overview of auditing for microbiological aspects of pharmaceutical and biopharmaceutical manufacturing. The use of cleanrooms to manufacture drug products has been done for years. Microbiological aspects of manufacturing have been incorporated into the manufacturing process. By understanding the microbiological aspect, auditors can....

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$193 Recorded (6 months unlimited access)
 
LSHCFJM003
Duration 90 mins
View Anytime
Joy McElroy  
FDA Inspections : What Regulations Expect

In this 90 minute webinar attendees will gain an understanding of the parameters, approaches, and concerns of FDA inspectors, and the tools for preparing, coping, and managing those inspections in the pharmaceutical, biologics, and med device facilities. Other objectives include inspection authorities and processes including 483s, warning letters, recalls, and other p....

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$193 Recorded (6 months unlimited access)
 
LSHCTJM001
Duration 90 mins
View Anytime
Joy McElroy  
Technical Writing for the Pharma, Biologics, and Medical Device Industry

This course addresses how to write effective correspondence ,reports, SOPs, and protocols in support of your company's activities.

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$193 Recorded (6 months unlimited access)
 
LSHCCP004
Duration 60 mins
View Anytime
Charles Paul  
Building a Compliant Documentation & Training System

This webinar will explore the area of training in regulated environments, its importance, and its relationship to compliance documentation. Training is one of the most underrated and least respected of all the disciplines found within modern manufacturing within regulated industries - foods, cosmetics, beverages, medical devices, pharmaceuticals, biologics, etc. Yet,....

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$193 Recorded (6 months unlimited access)
 
LSHCRPH001
Duration 60 mins
View Anytime
Paul Hales  
Ransomware and HIPAA - How to Prevent, Prepare, Respond, Recover

This course explains treacherous Ransomware threats attacking the Healthcare Industry and how to prevent, prepare for, respond to and recover from a Ransomware attack. It covers HIPAA Rules that apply to Ransomware, compliance with the HIPAA Rules and how to conduct a HIPAA Breach Risk Assessment to prove a Ransomware attack did not result in a Breach of Uns....

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$193 Recorded (6 months unlimited access)
 
LSHCBT008
Duration 90 mins
View Anytime
Brian L Tuttle  
HIPAA Enforcement - A Myths or Reality?

This lesson will be going into great detail regarding you practice or business information technology and how it relates to the HIPAA Security Rule, in particular portable devices.
Areas covered will be texting, email, encryption, medical messaging, voice data and risk factors as they relate to personal devices.
I will uncover myths versus reality as it relates ....

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$193 Recorded (6 months unlimited access)
 
HIPHLH001
Duration 75 mins
View Anytime
Laura S. Hargraves  
HIPAA Internal Audit Process & Policies: Your 1st Line of Defence

This course covers the components of an internal Audit process for HIPAA compliance. Why the audit is needed to support HIPAA compliance.What records are needed to ensure that your audit is replicable and supports your findings. Audits aspects which are crucial to ensure compliance,but can be pa....

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$193 Recorded (6 months unlimited access)
 
LSHCENK005
Duration 60 mins
View Anytime
Nathan A. Kottkamp  
Emergency Medical Treatment and Active Labour Act (EMTALA)

This webinar will examine the complexities and simplicities of EMTALA, the Emergency Medical Treatment and Active Labor Act. The webinar will distill the requirements of law, including its non-intuitive, highly-detailed definitions. The webinar will also discuss best practices for compliance and practical tips for compliance with the challenging situation of managin....

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$193 Recorded (6 months unlimited access)
 
LSHCEJK003
Duration 60 mins
View Anytime
Jeff Kasoff  
Elements of a Corrective and Preventive Action (CAPA) Program and Uses of CAPA Data

Year after year, CAPA is the subsystem cited most frequently during FDA inspections. A robust Corrective and Preventive Action (CAPA) program is of the utmost importance to a medical device manufacturer. A system that identifies and eliminates nonconformances and potential nonconformances enables both regulatory compliance and cost savings. This session will discuss t....

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$193 Recorded (6 months unlimited access)
 
LSHCHJ003
Duration 60 mins
View Anytime
Howard Jones  
The Roles And Responsibilities of a HIPAA Privacy and Security Officer

Discussions, presentation, and webinars regarding HIPAA regulations are usually addressed from the perspective of what the regulations entail, the necessity of compliance with the regulations, and the consequences of willful neglect or non-compliance.
This presentation addresses HIPAA regulations from a different perspective - from a personal perspective - from th....

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$193 Recorded (6 months unlimited access)
 
LSHCCEW001
Duration 60 mins
View Anytime
Edwin Waldbusser  
21 CFR part 11 Compliance - electronic records & electronic signatures

This Webinar will explain what 21 CFR Part 11 is, why it is important to FDA regulated companies and how conformance to Part 11 differs from just having good IT security. Procedures for controlling electronic signatures and electronic records will be explained. FDA regulated companies want to transition to electronic records for economy and efficiency. FDA, because of....

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$193 Recorded (6 months unlimited access)
 
LSHCMBI002
Duration 60 mins
View Anytime
Michael Brodsky  
Is it Method Verification or Validation, or Just Semantics

This Webinar will discuss the distinction between and requirements for method validation and method verification, to comply with ISO/IEC Standard 17025 for laboratory accreditation. Quantitative and Qualitative methods have different performance measurement requirements and require different statistical analyses. Although method validation and method verification are ....

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$193 Recorded (6 months unlimited access)
 
LSHCHNK004
Duration 60 mins
View Anytime
Nathan A. Kottkamp  
HIPAA And Litigation-Getting and Producing Records Through Discovery

This webinar will examine the interplay between HIPAA and state law when it comes to requesting and producing health records in the context of litigation. The webinar will address how attorneys should properly request health records and how covered entities and business associates should properly respond to such requests.

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$193 Recorded (6 months unlimited access)
 
LSHCSRC001
Duration 60 mins
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Roger Cowan  
Sterile Filtration of Pharmaceutical Products - Validation and Regulatory Requirements

Sterile filtration is one of the most critical steps in sterile pharmaceutical manufacture. This is because the filtration process provides the assurance of sterility in the finished drug product.
Therefore, the design, validation and ongoing monitoring of a sterile filtration system is essential for assuring the quality and safety of the pharmaceutical product.&nb....

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$193 Recorded (6 months unlimited access)
 
LSHCBT003
Duration 180 mins
View Anytime
Brian L Tuttle  
3-Hour Virtual Seminar on HIPAA Phase 2 Audits: How to be Prepared - An Insider's Perspective

I will be speaking to real life audits conducted by the Federal government for Phase 2 and beyond (I've been on both sides of these audits) what your highest risks are for being fined (some of the risk factors may surprise you). 
It seems almost daily I am receiving calls from nervous practice managers and compliance officers all over the USA regarding a HIPAA....

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$425 Recorded (6 months unlimited access)
 
LSHCHTS002
Duration 60 mins
View Anytime
Theresa K. Sheppard  
HIPAA: HIGHLIGHTS HOOPLA & HOOEY

Putting together a comprehensive HIPAA protocol and policyprogram can be a daunting task. In his course, learn the required changes to the Notice of Privacy Practices Form, the financial implications for willful neglect, why a daily data backup is no longer enough, and the communications that must not be sent via email or text. Gain a better understanding of the steps....

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$193 Recorded (6 months unlimited access)
 
LSHCMBI001
Duration 60 mins
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Michael Brodsky  
ISO/IEC 17025:2017 Update: Everything Old is New Again

Many laboratories have successfully developed and implementing a functional quality management system that not only complies with the management and technical requirements of ISO/IEC 17025:2005 but also meets their needs. Some are still struggling to get accredited and even those already accredited still have issues as evidenced by the number of non-conformances cited....

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$193 Recorded (6 months unlimited access)
 
LSHCHNK003
Duration 60 mins
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Nathan A. Kottkamp  
HIPAA Compliance in Light of Recent Enforcement Actions

This webinar will examine recent HIPAA enforcement actions and trends and will discuss practical insights on HIPAA from such enforcement activities. The webinar will cover HIPAA hot topics, as reflected in enforcement actions, and will provide guidance on avoiding enforcement actions.

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$193 Recorded (6 months unlimited access)
 
LSHCJPT004
Duration 60 mins
View Anytime
Jonathan P. Tomes  
What are Reasonable and Appropriate HIPAA Security Measures?

Often healthcare and related businesses do not understand that HIPAA is far more about policies and procedures than it is about technical security measures. The HIPAA Security Rule, for example, does not specify whether an entity must have a password system and, if it does, how many characters it must have and whether it has to be alphanumerical with one or more speci....

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$193 Recorded (6 months unlimited access)
 
LSHCBT007
Duration 90 mins
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Brian L Tuttle  
Why Should be Worried About HIPAA? All You Need to Know.

The objectives of this course will be to go over the specific risks associated with business associates as it relates to HIPAA compliance. I will uncover myths versus reality as it relates to this very enigmatic law based on over 1000 risk assessments performed as well as years of experience in dealing directly with the Office of Civil Rights HIPAA auditors. Times hav....

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$193 Recorded (6 months unlimited access)
 
LSHCBT006
Duration 90 mins
View Anytime
Brian L Tuttle  
How to conduct a HIPAA Security Risk Assessment and Write Policies?

This webinar will be addressing how practice/business managers (or compliance offers) need to get their HIPAA house in order before the imminent audits occur. It will also address major changes under the Omnibus Rule and any other applicable updates for 2017.
Areas also covered will be texting, email, encryption, medical messaging, voice data and risk factors ....

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$193 Recorded (6 months unlimited access)
 
LSHCJA010
Duration 60 mins
View Anytime
Jay Anstine  
Auditing for EMTALA Compliance

This webinar is designed to walk attendees through a process for auditing your organization's compliance with The Emergency Medical Treatment And Labor Act ("EMTALA"). More specifically, it will provide an overview of EMTALA, discuss key compliance challenges facing organizations who must comply, and discuss a step-by-step approach for routine and periodic auditing.

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$193 Recorded (6 months unlimited access)
 
LSHCCP003
Duration 60 mins
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Charles Paul  
Writing Effective Compliance Documentation

Compliance documentation to include Standard Operating Procedures - the documentation required by regulation - is essential to the effective and compliant running of any regulated business. Unfortunately, many individuals in those businesses miss the valuable opportunities that properly developed Standard Operating Procedures/Work Instructions can provide. Regulated d....

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$193 Recorded (6 months unlimited access)
 
LSHCBJK002
Duration 60 mins
View Anytime
Jeff Kasoff  
Best Practices in Supplier Management: How to meet FDA QSR and ISO 13485 requirements in a Lean, Cost-effective Manner

A lack of adequate control over purchases has resulted in a significant number of recalls due to component failures. Since FDA cannot regulate component suppliers, it is imperative that your company's purchasing and supplier control requirements provide the ass....

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$193 Recorded (6 months unlimited access)
 
LSHCHJ002
Duration 60 mins
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Howard Jones  
The Roles And Responsibilities of a HIPAA Privacy & Security Officer

Discussions, presentation, and webinars regarding HIPAA regulations are usually addressed from the perspective of what the regulations entail, the necessity of compliance with the regulations, and the consequences of willful neglect or non-compliance.
This presentation addresses HIPAA regulations from a different perspective - from a personal perspective - from th....

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$193 Recorded (6 months unlimited access)
 
LSHCSBT001
Duration 90 mins
View Anytime
Bryant Truitt  
Spotting a Weasel: The Personality of Dental Embezzler - 18 RED FLAGS!

Embezzler's view dental practices as "easy pickings" and have more time to work their schemes than doctors do to provide the management oversight they must today! After all, embezzlement is deception of exploiting vulnerabilities and coming up with schemes only limited by the weasel's imagi....

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$193 Recorded (6 months unlimited access)
 
LSHCBT009
Duration 90 mins
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Brian L Tuttle  
HIPAA Changes 2017

I will be speaking to real life situations I have personally dealt with on multiple occasions as part of HIPAA investigations relating to ransomware breaches. These can be absolutely devastating to your practice or business and can cause a major financial burde....

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$193 Recorded (6 months unlimited access)
 
LSHCJPT003
Duration 60 mins
View Anytime
Jonathan P. Tomes  
How to Perform a HIPAA Risk Analysis

Risk analysis is the key to implementing reasonable cost-effective security measures. And failure to conduct and update risk analyses are the single biggest cause of Health and Human Services imposed civil money penalties of up to several million dollars. And failure to conduct one has othe....

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$193 Recorded (6 months unlimited access)
 
LSHCJA009
Duration 60 mins
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Jay Anstine  
Telemedicine: Navigating Through Key Compliance Challenges

This webinar is designed to provide an overview of the common compliance challenges to delivering healthcare through telemedicine and offer strategies to ensure compliance. More specifically, Mr. Anstine will discuss issues such as state licensure, credentialing & privileging, liability insurance, reimbursement, establishing a physician-patient relationship, pati....

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$193 Recorded (6 months unlimited access)
 
LSHCLSH004
Duration 90 mins
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Laura S. Hargraves  
HIPAA Audits - Phase 2 What does this mean for you ?

The OCR HIPAA Audit program analyzes processes, controls, and policies of selected covered entities pursuant to the HITECH Act audit mandate. Will look at the process and whom it applies to. What the audits will focus on. Risk assessment will be reviewed and why this is important for your o....

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$193 Recorded (6 months unlimited access)
 
LSHCJPT002
Duration 60 mins
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Jonathan P. Tomes  
How to Write and Adopt HIPAA Policies and Procedures

Often healthcare and related businesses do not understand that HIPAA is far more about policies and procedures than it is about technical security measures. The HIPAA Security Rule, for example, does not specify whether an entity must have a password system and, if it does, how ....

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$193 Recorded (6 months unlimited access)
 
LSHCHNK002
Duration 60 mins
View Anytime
Nathan A. Kottkamp  
HIPAA For Employee Benefits Teams

This webinar will provide practical insights on HIPAA, including its applicability, its general rules, and requirements for compliance as it relates to employee benefits plans for companies, regardless of specific industry.

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$193 Recorded (6 months unlimited access)
 
LSHCJA013
Duration 180 mins
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Jay Anstine  
3-HR VIRTUAL SEMINAR ON Beyond the Allegation: How to Effectively Conduct Compliance Investigations.

This webinar will give attendees a blueprint for conducting effective compliance investigations, from A-Z. Given that responding to detected offenses are included in the Seven Elements of an Effective Compliance Program as deemed by the Office of Inspector General ("OIG"), this presentation is intended to provide strategies and tips for conducting and documenting inv....

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$425 Recorded (6 months unlimited access)
 
LSHCJPT001
Duration 60 mins
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Jonathan P. Tomes  
How to Handle HIPAA and HITECH Act Breaches, Complaints, and Investigations: Everything You Need to Know

This webinar will cover everything that you need to know about how to handle HIPAA security incidents, breaches, and complaints and the Department of Health and Human Resources Investigations thereof. Not all security incidents are breaches, but all....

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$193 Recorded (6 months unlimited access)
 
LSHCCP001
Duration 60 mins
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Charles Paul  
Managing for Compliance Effectiveness

Conforming to regulatory requirements, following all of the rules, and ensuring regulatory compliance is in no small part within the ability of the workforce to execute but in order to do this, the workforce must know what to do, how to do it, have the personal capacity to do it, have the tools to do it, and must be motivated to do it.

Performance management is....

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$193 Recorded (6 months unlimited access)
 
LSHCJME003
Duration 90 mins
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Joy McElroy  
Validation and Part 11 Compliance

This Computer System Validation Training course will explore proven techniques for reducing costs associated with implementing, using, and maintaining computer systems in regulated environments. Today, the FDA performs both GxP and Part 11 inspections, the Europeans have released an updated Annex 11 regulation that expands Part 11 requirements and companies must updat....

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$193 Recorded (6 months unlimited access)
 
LSHCML002
Duration 75 mins
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Max Lazar  
FDA GMP Requirements for API (Active Pharmaceutical Ingredients) - Just what do YOU need to do?

While this topic may appear easily addressed, appearances can be deceiving. This program will examine some history, real life experiences and discuss the real facts about GMP for Active Pharmaceutical ingredients. Just what is important to firms, producers of API and consumers of API. Discu....

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$193 Recorded (6 months unlimited access)
 
LSHCHNK001
Duration 60 mins
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Nathan A. Kottkamp  
HIPAA Basics for Non-Healthcare People

This webinar will provide a broad overview of HIPAA, including its applicability, its general rules, and requirements for compliance.

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$193 Recorded (6 months unlimited access)
 
LSHCBJK001
Duration 60 mins
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Jeff Kasoff  
Best Practices in Complaint Management: Complaint Handling in Compliance with FDA and ISO Regulations

Complaint handling is likely one of the more cross-functional parts of your quality system: Customer Service may receive your customer complaints, Sales and Marketing may need to reach out to the customer for additional information, Regulatory Affairs may determine whether the c....

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$193 Recorded (6 months unlimited access)
 
LSHCJM0001
Duration 90 mins
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Joy McElroy  
FDA Inspections: What Regulations Expect

In this 90 minute webinar attendees will gain an understanding of the parameters, approaches, and concerns of FDA inspectors, and the tools for preparing, coping, and managing those inspections in the pharmaceutical, biologics, and med device facilities. Other objectives include....

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$193 Recorded (6 months unlimited access)
 
LSHCBT004
Duration 180 mins
View Anytime
Brian L Tuttle  
3-HOUR VIRTUAL SEMINAR ON How to conduct a HIPAA Security Risk Assessment

This course will cover the proper methodologies on conducting a HIPAA Risk Assessment based on the formula used by Federal auditors and via the guidelines of the NIST (National Institute of Standard for Technologies). The course will also cover the most important aspects to be aware of in t....

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$425 Recorded (6 months unlimited access)
 
LSHCLSH003
Duration 180 mins
View Anytime
Laura S. Hargraves  
3-hour Virtual Seminar on OIG Work Plan 2017: Trends, Reports and Issues

Every year the OIG updates what it's focus is for the upcoming year. During this session we will look at the focus for OIG audits and oversight for 2017. These work plans often drive the audits that then occur within our work sites. They provided information that is beneficial f....

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$425 Recorded (6 months unlimited access)
 
LSHCBT001
Duration 180 mins
View Anytime
Brian L Tuttle  
3-hour Virtual Seminar On HIPAA Changes Under Omnibus

I will be speaking to real life situations I have personally dealt with on multiple occasions as part of HIPAA investigations relating to ransomware breaches. These can be absolutely devastating to your practice or business and can cause a major financial burden as well as embar....

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$425 Recorded (6 months unlimited access)
 
LSHCJA014
Duration 180 mins
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Jay Anstine  
3-hr Virtual Seminar on Compliance 101: Tackling the Common Realities You Will Encounter in the Profession.

This webinar will walk attendees through the most common political dilemmas facing any healthcare compliance professional on a daily basis no matter where they work in healthcare. In addition to identifying these common realities, Mr. Anstine will provide strategies, insights, a....

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$425 Recorded (6 months unlimited access)
 
LSHCDD001
Duration 60 mins
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Danielle DeLucy  
Achieving Success and Compliance in the Supply Chain

supply chain is a system of organizations, people, activities, information, and resources involved in moving a product or service from supplier to customer. Supply chain activities involve the transformation of natural resources, raw materials, and components into a finished product that is delivered to the end customer.

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$193 Recorded (6 months unlimited access)
 
LSHCJMAA002
Duration 90 mins
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Jose Mora  
An Advanced Course on Lean Documents, Lean Configuration and Document Control

In this Lean Documents, Lean Configuration, and Document Control training learn the different types of lean documents and the usage of lean document principles; types of controlled documents; examples of lean and non-lean controlled documents. Pros and cons of lean vs. non-lean documents.

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$193 Recorded (6 months unlimited access)
 
LSHCBT005
Duration 180 mins
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Brian L Tuttle  
3-HOUR VIRTUAL SEMINAR ON Ransomware and HIPAA - Be very careful here!

I will be speaking to real life situations I have personally dealt with on multiple occasions as part of HIPAA investigations relating to ransomware breaches. These can be absolutely devastating to your practice or business and can cause a major financial burden as well as embar....

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$425 Recorded (6 months unlimited access)
 
LSHCKO001
Duration 60 mins
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Kelly Ogle  
HIPAA for Medical and Dental Practices

This webinar covers privacy and security training for employees of private medical and dental practices and their business associates. The primary purpose is to fulfill HPAA's requirement for employee training and to improve HIPAA compliance.

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$193 Recorded (6 months unlimited access)
 
LSHCKO002
Duration 60 mins
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Kelly Ogle  
OSHA for Medical and Dental Practices

This webinar covers safety and health hazards typically found in private medical and dental practices. The primary purpose is to fulfill OSHA's requirement for employee training.

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$193 Recorded (6 months unlimited access)
 
LSHCNP001
Duration 60 mins
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Nagina Parmar  
Investigator initiated trials- What are we doing to ensure human subject protection?

This 1-hr virtual seminar will help you understand the key issues and challenges associated with investigator initiated trials. Investigator initiated trials are very important as they are important connection for the translation of research from bench to bedside. I will discuss the role of sponsor-investigator and ways we can ensure the protection of human subjects i....

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$193 Recorded (6 months unlimited access)
 
LSHC003
Duration 60 mins
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Joe Rosner  
Workplace Shootings: What You Need to Know Before, During, and After

In this online session, Joe Rosner, a nationally recognized expert on workplace violence and personal safety, you will gain insights in assessing and mitigating the risks of violence in the workplace. You'll learn the Who, What, Where and Why of workplace shooters. You will also....

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$193 Recorded (6 months unlimited access)
 
LSHCJM004
Duration 90 mins
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Jose Mora  
ISO 13485 2016 utilizing Principles of Lean Documents and Lean Configuration

All life science businesses are required to maintain their Quality Management System (QMS) processes in a state of control, via controlled documents and objective evidence in the form of records. Medical device designers and manufacturers are required to follow ISO 13485, and wi....

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$193 Recorded (6 months unlimited access)
 
LSHCJA007
Duration 60 mins
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Jay Anstine  
Looking Inward: Assessing the Effectiveness of Your Compliance Program

This webinar is designed to walk attendees through a self-assessment of the effectiveness of his/her compliance program to determine if the program is meeting the Federal government's standards (e.g. The Office of Inspector General's "Seven Elements of an Effective Compliance Pr....

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$193 Recorded (6 months unlimited access)
 
LSHCHJ001
Duration 60 mins
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Howard Jones  
The Requirements and Responsibilities of a HIPAA Security/Privacy Officer

Discussions, presentation, and webinars regarding HIPAA regulations are usually addressed from the perspective of what the regulations entail, the necessity of compliance with the regulations, and the consequences of willful neglect or non-compliance.
This presentation addresses HIPAA regulations from a different perspective - from a personal perspective - from t....

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$193 Recorded (6 months unlimited access)
 
LSHCJM002
Duration 90 mins
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Joy McElroy  
Process Validation for Pharma and Biologics Industries

This course will provide participants with a thorough understanding of the requirements of process validation for both small molecule (pharmaceuticals) and Biologic products. They will learn how to establish an effective process validation system and integrate it with other syst....

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$193 Recorded (6 months unlimited access)
 
LSHCSS002
Duration 90 mins
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Dr. Susan Strauss RN Ed.D  
Inclusion of LGBT Employees in Healthcare: Navigating Policies, Procedures, and Practices

Healthcare is a unique culture dealing with vulnerable patients and employees committed to quality patient care. However, research states that LGBT patients are treated in a more abusive manner than straight patients. How does the misconduct to LGBT patients impact your LGBT emp....

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$193 Recorded (6 months unlimited access)
 
LSHCJA006
Duration 60 mins
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Jay Anstine  
Compliance Program Infrastructure: The Basics Needed to Launch Your Compliance Program

This webinar is designed to provide an overview of the core infrastructure needed to launch a healthcare compliance program. More specifically, it will provide an overview of the Seven Elements of an Effective Compliance Program as deemed by the Federal government, and interpret....

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$193 Recorded (6 months unlimited access)
 
LSHCML001
Duration 75 mins
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Max Lazar  
Outsourcing and/or Purchasing API or Excipients - An Examination of Quality/Business Issues you should consider!

This program examines considerations that are important to firms that are considering if they should produce, outsource, or purchase API. The steps discussed during this program also have application to Excipients that are used by drug product producers. The subject has both Qua....

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$193 Recorded (6 months unlimited access)
 
LSHCSK0012
Duration 60 mins
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Srini Kolathur  
HOW TO MANAGE OCR/HHS HIPAA/HITECH AUDIT

Among other things, the HITECH Act significantly strengthened HIPAA enforcement activities. In addition to increasing penalties, allowing enforcement by state attorneys general, requiring notices of breaches, and making business associates directly subject to penalties, the HITECH Act mandated that Office for Civil Rights of HHS conduct HIPAA audits. This one-hour web....

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$193 Recorded (6 months unlimited access)
 
LSHCBT002
Duration 180 mins
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Brian L Tuttle  
3-HOUR VIRTUAL SEMINAR ON HIPAA: Upcoming Changes for 2017

This lesson will be addressing how practice/business managers (or compliance offers) need to get their HIPAA house in order as HIPAA is now fully enforced and the government is not using kid gloves any more. It will also address major changes under the Omnibus Rule and any other applicable updates for 2017 and beyond. There are an enormous amount of issues and risks f....

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$425 Recorded (6 months unlimited access)
 
LSHCSK001
Duration 60 mins
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Srini Kolathur  
HIPAA/HITECH ASSESSMENT FOR HEALTHCARE BUSINESS ASSOCIATES

As the compliance deadline for new HIPAA-HITECH rule approaches, it becomes imperative for healthcare business associate organizations to develop strategies to protect electronic health information, and comply with HIPAA-HITECH regulations. This instructor-led one-day training will teach you how to design, implement, and administer comprehensive healthcare IT complian....

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$193 Recorded (6 months unlimited access)
 
LSHCSS001
Duration 90 mins
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Dr. Susan Strauss RN Ed.D  
A New Civil Rights Law for Health Providers, Employees of Health Programs, and Health Insurance Companies: Section 1557 of the Affordable Care Act

Healthcare providers such as hospitals, clinics, physicians, community health centers, nursing homes, home care agencies, health insurance companies (including those found in the Health Insurance Marketplaces), and any other "covered entities" which....

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$193 Recorded (6 months unlimited access)
 
LSHCJM001
Duration 60 mins
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Jose Mora  
21 CFR Part 820 - Quality System Regulation - Applying Principles of Lean Documents and Lean Configuration

All life science businesses are required to maintain their Quality Management System (QMS) processes in a state of control, via controlled documents and objective evidence in the form of records. Medical device manufacturing plants, required to follow 21 CFR Part 820, have the a....

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$193 Recorded (6 months unlimited access)
 
LSHCPJB001
Duration 90 mins
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Peggy J Berry  
Preparing Compliant eCTD Submissions: Are you prepared for upcoming FDA mandate on e-submissions?

The international agreement to assemble all Quality, Safety and Efficacy information for a drug or biologic product into a common format (called the CTD - Common Technical Document) has improved the speed and efficiency for companies working in global development programs and clarified expectations by regulatory bodies. Reformatting for multiple submissions is substa....

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$193 Recorded (6 months unlimited access)
 
LSHCLSH002
Duration 75 mins
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Laura S. Hargraves  
HIPAA Internal Audit Process and Policies: Your 1st Line of Defence

This course covers the components of an internal Audit process for HIPAA compliance. Why the audit is needed to support HIPAA compliance.What records are needed to ensure that your audit is replicable and supports your findings. Audits aspects which are crucial to ensure compliance,but can be part of your daily activities ; reducing time and man hours needed. Why au....

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$193 Recorded (6 months unlimited access)
 
LSHCJA005
Duration 60 mins
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Jay Anstine  
Your First 100 Days as a Compliance Officer: Strategies to Prioritize Your Workload.

This webinar is designed to provide a realistic overview of what your first 100 days on the job as new compliance officer should look for any healthcare organization. It will discuss how to effectively on board to the organization and prioritize your workload for the first 100 days and beyond.

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$193 Recorded (6 months unlimited access)
 
FSPV003
Duration 90 mins
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Philip Vassallo  
Writing High-Profile Project Evaluation Reports

The reality of any professional discipline is this: If it is not in writing, it never happened. All the professional observation and objective review that a clinician puts into an analysis are meaningless unless the work appears in a complete, objective clear, and concise evaluation report. Knowing this truth is obvious; getting there is the challenge.

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$193 Recorded (6 months unlimited access)
 
LSHCCPA001
Duration 60 mins
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Carl Patterson  
Environmental Monitoring - Knowing your Cleanroom

This webinar will provide the proper methods and techniques required to maintain a clean room per FDA and ISO regulations. By the use of viable and non-viable testing, a cleanroom can be maintained. The results collected can determine the state of control the cleanroom operates on a continuous basis. In order to maintain a cleanroom, a proper cleaning agent rotation....

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$193 Recorded (6 months unlimited access)
 
LSHCWMC001
Duration 60 mins
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William Mack Copeland  
The Health Care Quality Improvement Act: How to Achieve Immunity

This webinar will discuss the Health Care Quality Improvement Act (HCQIA or the Act) in detail, including the standards that must be met to achieve immunity under the act. The HCQIA itself will be reviewed, including a detailed look at the Congressional purpose for the Act. The legislative history of the act will be reviewed to gain an understanding of the intent of ....

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$193 Recorded (6 months unlimited access)
 
LSHCNP002
Duration 60 mins
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Nagina Parmar  
Ethical Requirements & Development of Guidelines for Pediatric Trials in Developing Countries

This 1-hr virtual seminar will help you understand the key ethical issues and challenges associated with pediatric studies in developing countries. Pediatric populations in developing countries are extremely vulnerable participants in clinical research. I will discuss some of the key ethical issues and challenges associated with pediatric studies in developing countri....

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$193 Recorded (6 months unlimited access)
 
LSHCPJB002
Duration 90 mins
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Peggy J Berry  
SOP compliance management: A must for the pharmaceutical industry.

This workshop will explore what SOPs are, what they are used for, when they are required, how to write them effectively for compliance and for implementation within the organization, and how to ensure effective communication and training of procedures within the SOPs.

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$193 Recorded (6 months unlimited access)
 
LSHCJA004
Duration 60 mins
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Jay Anstine  
Compliance Challenges with Legalized Marijuana

This webinar is designed to provide an overview of the common challenges healthcare compliance officers must face in a world of legalized marijuana. More specifically, this presentation will begin with a brief summary of the regulatory history of marijuana in the United States and a survey of the states that have currently legalized marijuana for recreational purpose....

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$193 Recorded (6 months unlimited access)
 
LSHCEW001
Duration 60 mins
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Edwin Waldbusser  
Hazard Analysis following ISO 14971

Designing a medical device and testing it to prove that it works is not sufficient in the eyes of the FDA to provide a safe product for users. The FDA has determined, through analysis of product recall data that the majority of recalls were due to a faulty design process. These recalled products were tested before release and later found to fail in unanticipated ways ....

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$193 Recorded (6 months unlimited access)
 
LSHCJM00113
Duration 60 mins
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Jose Mora  
Creation of DHFs, DMRs, and DHRs utilizing the principles of Lean Documents and Lean Configuration

The Theory of Lean Documents is the product of applying lean principles to the creation, design, process, and management of controlled documents typically found in regulated industries. Just as lean principles challenge traditional process concepts and "push" systems, many traditional document practices are artifacts of a flawed approach. Lean documents presents a ....

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$193 Recorded (6 months unlimited access)
 
LSHCJA012
Duration 60 mins
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Jay Anstine  
Navigating the Compliance Challenges with Holiday Gifts

This webinar is designed to help attendees navigate through the compliance challenges related to holiday gift giving and receiving with physicians, vendors, patients, and co-workers. More specifically, it will discuss the regulatory framework surrounding gifts, common gifting scenarios, the pitfalls to avoid, and strategies for drafting organizational gift policies.

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$193 Recorded (6 months unlimited access)
 
LSHCGS002
Duration 60 mins
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Gregory J Simms  
A Legal Compliance Program When Billing Durable Medical Equipment

Learn that treating your Medicare patients with Durable Medical Equipment can be great for patient clinical outcomes, a great revenue stream and can be legally compliant. It will also lower healthcare costs. However one must know how to get the proper licensure and know the Federal & State Guidelines. This webinar will walk you through the process of how to do the....

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$193 Recorded (6 months unlimited access)
 
LSHCCT003
Duration 90 mins
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Carolyn Troiano  
FDA Compliance and Laboratory Computer System Validation

You should attend this seminar if you are responsible for planning, executing or managing the validation of laboratory computer systems governed by FDA regulations.
Effective and compliant computer system validation is critical to any FDA-regulated organization. During the past 30 years, best practices have been developed that, if followed, can ensure laboratory c....

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$193 Recorded (6 months unlimited access)
 
LSHCCP001
Duration 90 mins
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Charles Parker  
New Technologies Affecting Healthcare

This course covers the new technologies affecting healthcare. During this discussion, we will look at how IoT, data analysis and advanced AI is enhancing the outcomes of individuals as well as driving new engagement models outside of the traditional care environments. As the shifting payment models are driving from fee-for-service to paying for quality outcomes, the ....

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$193 Recorded (6 months unlimited access)
 
LSHRC003
Duration 60 mins
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Roger Cowan  
HVAC and GMP Environmental Control - for Pharmaceutical Clean Rooms

Environmental control of pharmaceutical clean rooms is essential to the manufacture of a quality product. Control of such conditions as airborne particulate, microorganisms, temperature, humidity, differential pressure, airflow, air velocity and personnel is crucial to protect the product from contamination. 
Therefore, the design, validation and ongoing monit....

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$193 Recorded (6 months unlimited access)
 
LSHCLSH001
Duration 60 mins
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Laura S. Hargraves  
2017 Proposed Home Health PPS Rule: Pre-Payment Review and Other - Regulatory Developments

The HH PPS proposed rule is one of the several rules for calendar year 2017 that reflect a broader Administration-wide strategy to create a health care system that results in better care, smarter spending, and healthier people. Provisions in these rules are helping to move our health-care system to one that values quality over quantity and focuses on reforms such....

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$193 Recorded (6 months unlimited access)
 
LSHCRC004
Duration 60 mins
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Roger Cowan  
Sterile Filtration of Pharmaceutical Products - Validation and Regulatory Requirements

Sterile filtration is one of the most critical steps in sterile pharmaceutical manufacture. This is because the filtration process provides the assurance of sterility in the finished drug product.
Therefore, the design, validation and ongoing monitoring of a sterile filtration system is essential for assuring the quality and safety of the pharmaceutical product. ....

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$193 Recorded (6 months unlimited access)
 
LSHCTF001
Duration 60 mins
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Thomas J. Force  
Federal Case Law that Out-of-Network Providers Need to Know

This presentation will explore the lawsuits brought by and against health plans and health insurers against and by out-of-network Ambulatory Surgery Centers, Hospitals and other healthcare providers affecting revenue. Cases explored will include those involving balance billing issues, recoupments, assignment of benefits (legal standing) and other issues affecting the....

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$193 Recorded (6 months unlimited access)
 
LSHCJA003
Duration 60 mins
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Jay Anstine  
How to Effectively Consult to Physicians and Healthcare Leaders on Compliance issues.

This webinar is designed to provide strategies and insights for effectively consulting to physicians and healthcare leaders on compliance issues. It will cover how to think and act like a consultant, a consistent process for consulting and strategies for communicating with disengaged physicians and leaders to improve buy-in. Using a case scenario, this presentation....

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$193 Recorded (6 months unlimited access)
 
LSHCMB001
Duration 90 mins
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Michael Brodsky  
Understanding and implementing an effective laboratory Quality Management System to comply with ISO/IEC 17025

QMS is the catch phrase for accreditation and is the backbone of ISO/IEC Standard 17025:2005. Accreditation to international standards is being becoming the norm in the global analytical community. Although essentially voluntary, there are many jurisdictions that now require foo....

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$193 Recorded (6 months unlimited access)
 
LSHCJW003
Duration 60 mins
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Joseph Wolfe  
Structuring Physician Recruitment and Non-Physician Practitioner Support Arrangements Under the New 2016 Stark Rules.

In this session Mr. Wolfe will provide a general Stark Law overview. He will also discuss best practices for auditing existing recruitment arrangements and for implementing new NPP support arrangements under the new 2016 Stark rules.CMS recently finalized a number of significant....

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$193 Recorded (6 months unlimited access)
 
LSHCJA002
Duration 60 mins
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Jay Anstine  
Clear, Complete, and Concise: Strategies for Writing an Investigation Report

This webinar provides a blueprint for how to effectively draft a compliance investigation report. Given the frequent occurrence that compliance officers find themselves in with having to respond to identified issues through an investigation, this presentation is intended to help attendees apply a consistent approach for drafting an investigation report that can be d....

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$193 Recorded (6 months unlimited access)
 
LSHCJF001
Duration 90 mins
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Janette Levey Frisch  
Making Sense of the FMLA, ADA and Workers Comp Overlap

Few employers can say they have never had challenges with leave of absence issues. Virtually every employer in every sector of the American (and global) economy has. The Family Medical Leave Act (FMLA) requires covered employers to allow eligible employees up to 12 weeks of unpa....

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$193 Recorded (6 months unlimited access)
 
LSHRC002
Duration 60 mins
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Roger Cowan  
Pharmaceutical Compressed Air - Quality GMP Standards and Requirements

Compressed air for pharmaceutical use is considered a critical utility as many of its applications involve direct contact with the pharmaceutical product.
The design, construction and monitoring of a compressed air system is essential for maintaining a quality system without contamination of the product. 
Proper testing of compressed air quality according t....

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$193 Recorded (6 months unlimited access)
 
LSHCJA001
Duration 75 mins
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Jay Anstine  
Compliance with Section 1557 of the Affordable Care Act: Non-discrimination

Section 1557 of the Affordable Care Act ("ACA") is the civil rights provision prohibiting discrimination on the basis of race, color, national origin, sex, age, or disability in certain health programs and activities. This new federal rule became effective on October 17, 2016.

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$193 Recorded (6 months unlimited access)
 
LSHCCT002
Duration 90 mins
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Carolyn Troiano  
Organizational Change Management (OCM) Best Practices for Computer Systems Regulated by FDA

This course is intended to provide specific guidelines for coaching attendees on the best practices for creating organizational change as it relates to computer systems regulated by FDA. These include, but are not limited to system implementation, testing, validation, migration,....

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$193 Recorded (6 months unlimited access)
 
LSHCGS001
Duration 60 mins
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Gregory J Simms  
A Durable Medical Equipment Revenue Program Every Practice Should Have

Increased Revenue & Profit For Your Practice!
Better Service & Outcomes For Your Pati....

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$193 Recorded (6 months unlimited access)
 
LSHCDD004
Duration 60 mins
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Danielle DeLucy  
Managing SOP Compliance per FDA Regulations

Standard Operating Procedures (SOPs) are a regulatory requirement for industries that are governed by the FDA and other world health authorities. Currently, there is no guidance on how to develop or manage the SOP creation or the SOP quality system.

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$193 Recorded (6 months unlimited access)
 
LSHCESVM001
Duration 60 mins
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Elina Sabilova & Alla Keinig  
What will happen to your practice if you continue using unspecified codes?

Short-term and long-term consequences of using unspecified codes.

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$193 Recorded (6 months unlimited access)
 
LSHCHC002
Duration 180 mins
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Howard Cooper  
3-hr Virtual Seminar on An overview of the pharmaceutical manufacturing cycle: ICH Q7A, GMP for pharmaceutical active ingredients (PAI) and Part 210-211 Current Good Manufacturing Practices for Finished Pharmaceuticals

This webinar focuses on the GMP quality system of the drug manufacturing cycle beginning with ICH Q7A, Good Manufacturing Practice Guidance for Active Pharmaceutical Ingredients then focusing on 21 CFR Part 210-211 Current Good Manufacturing Practices for Finished Pharmaceutical....

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$397 Recorded (6 months unlimited access)
 
LSHC0020
Duration 90 mins
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Brian L Tuttle  
HIPAA Phase 2: Keys to Surviving an Audit

HIPAA NOW HAS TEETH! Phase 2 Audits and personal patient remedies have changed the landscape!
This once relatively benign legislation is being fully enforced and the news is not good f....

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$193 Recorded (6 months unlimited access)
 
LSHC0016
Duration 75 mins
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Jay Anstine  
Legislative and Regulatory Enforcement Update

This session would provide a general overview of regulatory developments impacting the business of healthcare as well as trends in enforcement from the government's perspective.  It will primarily focus on fraud and abuse and patient privacy, but may also include other selected topics depend....

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$187 Recorded (6 months unlimited access)
 
LSHRC001
Duration 60 mins
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Roger Cowan  
CMO Supplier Quality Agreements - How to Comply with new FDA and EU Guidelines for Contract Drug Manufacture

A Quality Agreement is a contract between a pharmaceutical firm and a GMP Contract Manufacturer detailing the responsibilities of each party in assuring the quality, safety and efficacy of the manufactured drug.
Recently, the EU and the FDA issued regulatory guidance to bring some clarity and consistency to these quality contracts:

  • EU GMP Chapter 7 "Out....

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$193 Recorded (6 months unlimited access)
 
LSHCJW002
Duration 60 mins
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Joseph Wolfe  
Structuring Physician Leases Under the New 2016 Stark Rules

In this session Mr. Wolfe will provide a general Stark Law overview. He will also discuss best practices for auditing existing space lease arrangements and for implementing new time-share arrangements under the new 2016 Stark rules.

Background:
CMS recently finalized a number of significant changes to the Stark Law for....

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$193 Recorded (6 months unlimited access)
 
LSHC0019
Duration 90 mins
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Brian L Tuttle  
Patients Suing under HIPAA - Beware of New Laws

There are major changes to HIPAA set forth by the Federal government whereby patients can receive remedies for HIPAA violations! Omnibus has changed the HIPAA landscape for good! State laws are now in place increasing liability for patient remedies! This once rarely enforced law has changed and you need to know what's going on! What factors might spurn a HIPAA audit? ....

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$193 Recorded (6 months unlimited access)
 
LSHCCT006
Duration 90 mins
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Carolyn Troiano  
FDA's Latest Regulations for Tobacco Industry Effective 8/2016

The Tobacco Control Act went into effect by FDA on June 22, 2009. Through this ruling, the FDA regulated cigarettes, cigarette tobacco, roll-your-own tobacco and smokeless tobacco, but in 2016, the FDA finalized a rule, Deeming Tobacco Products To Be Subject to the Federal Food,....

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$193 Recorded (6 months unlimited access)
 
LSHCVS011
Duration 180 mins
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Brian L Tuttle  
3-Hr Virtual Training: What to Expect in a Federal HIPAA Audit and How to Avoid an Audit Altogether

Brian will discuss changes with the Health and Human Services in regards to the enforcement of the HIPAA laws already on the books and new risks specific to business associates. It will also discuss factors that might cause an unwanted visit or letter from the Office of Civil Ri....

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$397 Recorded (6 months unlimited access)
 
LSHC0018
Duration 90 mins
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Brian L Tuttle  
HIPAA Phase 2 Audits - an inside look at what to expect

HIPAA NOW HAS TEETH! Phase 2 Audits and personal patient remedies have changed the landscape!
This once relatively benign legislation is being fully enforced and the news is not good f....

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$193 Recorded (6 months unlimited access)
 
LSHCJW001
Duration 60 mins
View Anytime
Joseph Wolfe  
Auditing Physician Contracts Under the New 2016 Stark Rules

In this session Mr. Wolfe will provide an overview of the Stark Law and its 2016 changes. He will also discuss best practices for implementing and auditing physician compensation arrangements to minimize liability exposure and penalties, including conducting compliance audits, i....

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$193 Recorded (6 months unlimited access)
 
LSHC0017
Duration 90 mins
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Brian L Tuttle  
WHY YOU SHOULD BE WORRIED ABOUT HIPAA: A Boot Camp

Are you confused about HIPAA? Do you just want the basics and in plain English? 
Do you know there are civil and criminal penalties even for the rank and file staff member!....

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$193 Recorded (6 months unlimited access)
 
LSHC0022
Duration 60 mins
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Debra L. Phairas  
Closing A Medical Practice

This workshop will discuss the ethical and legal tasks to close a practice. There are many tasks that must be accomplished and having an organized plan is essential.  

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$193 Recorded (6 months unlimited access)
 
LSHC0007
Duration 60 mins
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Jay Anstine  
Beyond the Allegation: How to Effectively Conduct Compliance Investigations

This presentation provides a blueprint for how to conduct an effective compliance investigation. Since responding to detected offenses and developing corrective action plans are included in the Seven Elements of an Effective Compliance Program, this presentation is intended to aid compliance professionals with a consistent approach for conducting investigations, fro....

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$193 Recorded (6 months unlimited access)
 
LSHC0005
Duration 60 mins
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Edwin Waldbusser  
Human Factors /Usability Study based on ISO 62366 and latest FDA Guidance.

Human Factors/ Usability is the analysis of how people interact with medical devices. The process of conducting rigorous human factors studies throughout the design process, integrating it with the device risk analysis and design process, and validating the effectiveness of the studies will be explained. The variou....

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$193 Recorded (6 months unlimited access)
 
LSHC0014
Duration 90 mins
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Jay Anstine  
HIPAA Breach Notification Rule: A Blueprint for Conducting Consistent Risk Assessments

This presentation will cover developing a blueprint for conducting risk assessments under the HIPAA Breach Notification Rule. More specifically, it will address topics such as what constitutes a breach, what to include in a Breach Notification policy, how to conduct a risk assessment analyzing any issue, and how to document your risk assessment. It will conclude wit....

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$187 Recorded (6 months unlimited access)
 
LSHC0002
Duration 60 mins
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Jason Teliszczak  
Medical Devices - ISO 13485 - Do you really know what you need to?

ISO 13485 is for medical devices. So anyone that is currently or wants to develop components for and/or entire medical device products, they need to meet local regulatory as well as ISO 13485 standards.

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$193 Recorded (6 months unlimited access)
 
LSHC0004
Duration 60 mins
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Edwin Waldbusser  
How to Prepare for a FDA inspection and prepare response to 483's and warning letters.

In this webinar you will learn about the types of FDA inspections, preparations such as assigning dedicated personnel to specific tasks for the inspection, facility requirements to support the inspection  (front room, back room), the value of mock audits, how personnel should conduct themselves, the inspection process and how to respond to 483's and warning lette....

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$193 Recorded (6 months unlimited access)
 
LSHC0008
Duration 60 mins
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Jay Anstine  
Tracking Physician Gifts Under The Stark Non-Monetary Compensation Rule


The Stark law generally prohibits physicians from referring Medicare patients for designated health services ("DHS") to an entity the physician or immediate family member has a financial relationship with, unless an exception applies. Under Stark, there is an exception known as the Non-Monetary Compensation ("NMC") exception (42 C.F.R. 411.357(k) that allows DHS ....

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$193 Recorded (6 months unlimited access)
 
LSHC0013
Duration 90 mins
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Jay Anstine  
Compliance 101: Common Realities You Will Encounter As a Compliance Officer

This presentation will provide insights on common dilemmas that any healthcare compliance professional faces no matter where they work in healthcare. In addition to identifying the common realities, this presentation also provides strategies and tips to help overcome each reality in order to succeed in the role. The presentation will leave time at the end of questio....

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$187 Recorded (6 months unlimited access)
 
LSHC00017
Duration 60 mins
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Jay Anstine  
HIPAA and the front office

HIPAA audits are on the rise, and you'll probably be surprised to learn that you are most likely to be targeted for a HIPAA audit based on a patient compliant. And your front desk could be a target area. And not always for the reasons you'd think.

HIPAA compli....

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$193 Recorded (6 months unlimited access)
 
LSHC0015
Duration 60 mins
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Jay Anstine  
How to Draft a Memorandum Analyzing Any Regulatory Issue

This presentation provides a blueprint for how to draft a written opinion analyzing any regulatory issue.  Since analyzing issues is central to what a compliance officer does on a daily basis, this presentation is intended to aid compliance professionals with how to analyze an issue and comm....

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$193 Recorded (6 months unlimited access)
 
LSHC002
Duration 60 mins
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Joe Rosner  
Workplace Violence Personal Safety Training

Workplace Violence in your workplace; the consequences are many, unpredictable, and can be severe. Injury or death of employees, customers, and/or visitors, lawsuits, property damage, increased insurance premiums, OSHA enforcement actions, increases employee turnover and reduced community trust. Mass shootings in the workplace and victim total....

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$193 Recorded (6 months unlimited access)
 
VMHCLSC001
Duration 180 mins
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Brian L Tuttle  
3-hour Virtual Seminar on HIPAA Survival: What you need to know?

Brian will uncover myths versus reality as it relates to this very enigmatic law based on over 1000 risk a....

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$395 Recorded (6 months unlimited access)
 
HCLSBT002
Duration 90 mins
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Brian L Tuttle  
HIPAA Changes 2016 and How to Comply?

The objectives of this course will be to demonstrate from real life audits conducted by the Federal government what your highest risks are for being fined (some of the risk factors may surprise you). In addition, this course will cover the highest risk factors for being sued by patients for wrongful disclosures of PHI. The course will also cover the manner i....

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$193 Recorded (6 months unlimited access)
 
HCLS003
Duration 90 mins
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Brian L Tuttle  
HIPAA Changes and How to Comply?

This lesson will be addressing how practice managers (or compliance offers) need to get their HIPAA house in order before the imminent audits occur. It will also address major changes under the Omnibus Rule and any other applicable updates for 2015 and 2016. There are an enormous amount of issues and risks for covered entities and business associates under Omnibus, fi....

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$187 Recorded (6 months unlimited access)
 
HCLS010
Duration 90 mins
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Jerry Dalfors  
cGMP Application for Design & Operation

GMP was established back in the 60's and 70's to help Drug and Medical Device companies set up systems and related employee activities to help minimize patient risks.cGMP (current Good Manufacturing Practices needed to minimize patient risk and increase the probability of profitability) regulations require a quality related operations system that establishes and maint....

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$178 Recorded (6 months unlimited access)
 
HC0008
Duration 90 mins
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Brian L Tuttle  
How to conduct an HIPAA Risk Assessment and Write Policies

This lesson will clearly outline the proper methodology and importance of conducting a HIPAA Security Risk Assessment

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$189 Recorded (6 months unlimited access)
 
HLS001
Duration 90 mins
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Brian L Tuttle  
Preparing For Imminent Federal HIPAA Audits

This webinar will be hitting on the changes regarding HIPAA and why the tenured staff members need to be very clear on the risks involved (and personal responsibility) of securing private health information

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$195 Recorded (6 months unlimited access)
 
HC0015A
Duration 90 mins
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Brian L Tuttle  
IT and HIPAA (Level: Advance)

This lesson will be going into the basics regarding you practice or business information technology and how it relates to the HIPAA Security Rule. Areas covered will be system auditing, encryption, physical security, IT consulting firms, disaster recovery, web based vs in-house systems, and risk factors as they relate to IT.
In addition I will be covering why you S....

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$193 Recorded (6 months unlimited access)
 
HC0114I
Duration 90 mins
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Brian L Tuttle  
IT and HIPAA (Level: Intermediate)

This lesson will be going into great detail regarding you practice or business information technology and how it relates to the HIPAA Security Rule. Areas covered will be system auditing, encryption, physical security, IT consulting firms, disaster recovery, web based vs in-house systems, and risk factors as they relate to IT.In addition I will be covering why you SHO....

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$187 Recorded (6 months unlimited access)
 
HC0009B
Duration 90 mins
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Brian L Tuttle  
Why You Should be Worried About HIP