Classifying Medical Devices


Charles H. Paul is Keynote Speaker at Compliance key Inc. He is President of C. H. Paul Consulting, Inc. - a regulatory, training, and technical documentation consulting firm. Charles is a management consultant, instructional designer and regulatory consultant and has led C. H. Paul Consulting, Inc. since its inception over 25 years ago. He regularly consults with Fortune 500 pharmaceutical, medical device, and biotechnology firms assisting them in achieving human resource, regulatory, and operational excellence. He is a regular presenter of webinars and on-site seminars in a variety of relate........

Overview

The Food and Drug Administration (FDA) has established classifications for approximately 1,700 different generic types of devices and grouped them into 16 medical specialties referred to as panels. Each of these generic types of devices is assigned to one of three regulatory classes based on the level of control necessary to assure the safety and effectiveness of the device.

The determination process, how you apply the classification process to your device, is complex and requires several levels of analysis to make the proper device classification.

Proper medical device classification is the fundamental first step in submitting your device for approval anywhere in the world.

This webinar will detail the medical device classification process for the United States through the FDA and will overview the very complex process for medical device classification within the EU. Specifically, this webinar will provide detailed background into the process and will make clear some of the very complex terms and sub-processes associated with medical device classification. We will actually work through the classification process step-by-step for the US and will overview how the process is accomplished for the EU.

Why should you attend this webinar?

When designing and developing medical devices it is essential to properly classify your device early on in the process to prevent costly and cumbersome regulatory issues and added or unnecessary work later in the design and development process.

What is the impact? What is the cost? Making the wrong decision - assigning your device a higher classification than necessary within any market, can cost you significant time and money in terms of your submittal process and how the design, development, and the management of your device will be executed over its lifecycle.

Areas Covered in the Session:

Who can Benefit:

Anyone involved in the design, development, marketing, submittal, and approval of medical devices that has had some exposure to the subject area and regulated environments.



Webinar Id: LSHCCP005

Training Options:

Duration: 60 mins

 Recorded: [Six month unlimited access]

 $237(Single Attendee)  $599(Unlimited Attendee)

Refund Policy
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