Date: 5th Nov 2014
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. Click link to view.download printable slides of respective webinar
- 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 Program
- 2:00-3:00 pm: Corrective and Preventive Actions (CAPA) Basics
- 3:00-4:00 pm: Electronic Medical Device Reporting (eMDR) 21 CFR Part 803
Target Audience included experts and professionals from Medical Device Industry, Medical Device Developers, Medical Device Industry Associations.
No comments:
Post a Comment