CPG and Retail


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 Webinar Id:  CKHDD001
 10:00 AM PT | 01:00 PM ET
 01/26/2018
 Duration: 60 mins

How to properly investigate OOS/OOT Results

This webinar will review the regulatory requirements for investigating an OOS Investigation. The responsibilities of the analyst, the supervisor and QA will be discussed. A detailed flow chart will be used to help the attendees clearly understand the steps and the order in which they are to be performed. The structure of an Investigation report which properly documents the investigation will be discussed.


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       $179
  Single Attendee
(Only for one Participant)
     $363
Multiple Attendee
( 2 - 5 Participants)
     $726
Corporate Attendee
( 6 - 10 Participants)
       $237
    Recorded
(6 months unlimited access)
 Webinar Id:  CKUDD002
 10:00 AM PT | 01:00 PM ET
 02/09/2018
 Duration: 60 mins

Understanding Aseptic Technique and Cleanroom Behavior

Compounding sterile products are made utilizing aseptic technique. Aseptic technique is a microbiological term referring to the prevention of microorganism contamination. The procedure involves the use of specialized equipment, sterile apparel, meticulous processing, and continuous cleaning.


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       $179
  Single Attendee
(Only for one Participant)
     $363
Multiple Attendee
( 2 - 5 Participants)
     $726
Corporate Attendee
( 6 - 10 Participants)
       $237
    Recorded
(6 months unlimited access)
 Webinar Id:  CKDCT002
 10:00 AM PT | 01:00 PM ET
 02/12/2018
 Duration: 90 mins

Data Governance for Computer Systems Regulated by FDA

Effective and compliant computer system data management is critical to organisations in the pharmaceutical, biologic, vaccines, tobacco, animal health, medical device or other FDA-regulated industry. During the past 30 years, best practices have been developed to ensure computer systems used in these environments can be cost-effectively managed while meeting all aspects of FDA compliance. To take this a step further, we are now looking ........


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       $179
  Single Attendee
(Only for one Participant)
     $363
Multiple Attendee
( 2 - 5 Participants)
     $726
Corporate Attendee
( 6 - 10 Participants)
       $237
    Recorded
(6 months unlimited access)
 Webinar Id:  CKIC001
 10:00 AM PT | 01:00 PM ET
 03/16/2018
 Duration: 90 mins

Integration of ERP and Legacy Computer Systems Regulated by FDA

We will discuss the importance of applying industry best practices when planning, executing and validating the integration of a legacy system with a business system, such as an ERP or similar type of enterprise or supply-chain automation system. These are commonly integrated in manufacturing companies that use large-scale, enterprise-wide solutions for automating the production, testing and distribution processes in pharmaceutical, biot........


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       $179
  Single Attendee
(Only for one Participant)
     $363
Multiple Attendee
( 2 - 5 Participants)
     $726
Corporate Attendee
( 6 - 10 Participants)
       $237
    Recorded
(6 months unlimited access)
 Webinar Id:  CKFDD003
 10:00 AM PT | 01:00 PM ET
 03/19/2018
 Duration: 60 mins

FDA's Expectations from Supplier Management for GMP: Quality Agreements and More.

When contemplating the use of a supplier you would normally have many requirements and expectations that must be met. These include technical, regulatory, quality, responsiveness, location, readiness, and those less defined but critical. One of the tools at your disposal to verify the supplier's acceptability is to audit its operation. This webinar is designed to provide the participants a working knowledge of supplier audits. The why, ........


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       $179
  Single Attendee
(Only for one Participant)
     $363
Multiple Attendee
( 2 - 5 Participants)
     $726
Corporate Attendee
( 6 - 10 Participants)
       $237
    Recorded
(6 months unlimited access)
 Webinar Id:  CKADD004
 10:00 AM PT | 01:00 PM ET
 04/05/2018
 Duration: 60 mins

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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       $179
  Single Attendee
(Only for one Participant)
     $363
Multiple Attendee
( 2 - 5 Participants)
     $726
Corporate Attendee
( 6 - 10 Participants)
       $237
    Recorded
(6 months unlimited access)
 Webinar Id:  CKADD005
 10:00 AM PT | 01:00 PM ET
 05/24/2018
 Duration: 60 mins

Applying Quality Risk Management

This webinar is intended to help you better understand and get familiar with best practices for FDA approval process for quality risk management (QRM) applicable for pharmaceutical industry. This webinar is further intended to discuss how risk management plans can be effectively integrated into a quality system (QS) in the pharmaceutical industry.


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       $179
  Single Attendee
(Only for one Participant)
     $363
Multiple Attendee
( 2 - 5 Participants)
     $726
Corporate Attendee
( 6 - 10 Participants)
       $237
    Recorded
(6 months unlimited access)
 Webinar Id: CR0011
 View Anytime
 Duration: 60 mins

Bioterrorism, Food Fraud and Food Security - A Cultural Conundrum

Intentional contamination or adulteration of food is a reality. We will review some examples of the dire consequences of adulteration ostensibly for economic gain This webinar will also discuss the potential threats of using food as biological weapon and the actions food companies can take to mitigate and minimize the risks of food bioterrorism.

$237  Recorded  (6 months unlimited access)

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 Webinar Id: FD0003
 View Anytime
 Duration: 60 mins

Verification or Validation of Methods in Food Microbiology

The Webinar will discuss the distinction between and requirements for method validation and method verification, to comply with ISO/IEC Standard 17025:2005 for a microbiology laboratory accreditation

$237  Recorded  (6 months unlimited access)

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 Webinar Id: FD0002
 View Anytime
 Duration: 60 mins

Measurement Uncertainty in Microbiology

The Webinar will discuss the concept and application of uncertainty of measurement (MU) as required by ISO/IEC Standard 17025:2005 for laboratory accreditation, from a practical microbiological perspective, using unambiguous language with useful examples.

$237  Recorded  (6 months unlimited access)

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