Webinar: CDRH Industry Basics Workshop
Summary: This workshop (presented by webinar) will provide information on the fundamental concepts of medical device regulations.
The
workshop will feature five sessions, each of which will consist of a
presentation followed by a question and answer session with a panel of
experts. Participants will be able to email or call us with your
questions during each session.
Participants can choose to
participate in any and/or all of the sessions. Each session will begin
precisely at the scheduled time.
- 10:00-11:00 am: Investigational Device Exemption (IDE) Program
- 11:00-12:00 noon: 510(k) Program
- 12:00-1:00 pm: De Novo
- 2:00-3:00 pm: Corrective and Preventive Actions (CAPA)
- 3:00-4:00 pm: Electronic Medical Device Reporting (eMDR)
Target Audience: Medical Device Industry, Medical Device Developers, Medical Device Industry Associations
Webinar Details
Date: November 4, 2014
Time: 10:00 AM – 4:00 PM, Eastern Time – To ensure you are connected, log-in by 9:45 AM.
Webinar Link: http://fda.yorkcast.com/webcast/play/c369da3174e945db99747267beeb2a551d
Audio Dial-In: 800-527-1401 (to ask questions during the Q&A sessions)
Webinar Link: http://fda.yorkcast.com/webcast/play/c369da3174e945db99747267beeb2a551d
Audio Dial-In: 800-527-1401 (to ask questions during the Q&A sessions)
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