Join the FDA on July 14, 2016, from 2:00 – 3:30 PM (Eastern Time), for an update on two key activities from the CDRH Office of Device Evaluation Clinical Trials Program:
- Early Feasibility Studies
- Draft Guidance: FDA Categorization of Investigational Device Exemption (IDE) Devices to Assist the Centers for Medicaid Services (CMS) with Coverage Decisions
Webinar Details
Registration is not necessary; however we expect high interest in the event and recommend you connect to the webinar at least 15 minutes prior to the webinar start time.
Date: July 14, 2016
Time: 2:00 PM – 3:30 PM, Eastern Time
To ensure you are connected, log-in by 1:45 PM.
Time: 2:00 PM – 3:30 PM, Eastern Time
To ensure you are connected, log-in by 1:45 PM.
To hear the presentation and ask questions:
Dial: 877-917-9491; Passcode: 599543
International: 1-212-287-1619; Conference number: PW1052941
Dial: 877-917-9491; Passcode: 599543
International: 1-212-287-1619; Conference number: PW1052941
To view the slide presentation during the webinar: https://www.mymeetings.com/nc/
If you are unable to connect with the link above, use the following link to view the slides: https://www.livemeeting.com/
Following the webinar, a transcript, recording and slides will be available at: http://www.fda.gov/CDRHWebinar
NOTE: The FDA does not provide Continuing Education (CEU) or Certificates of Attendance for webinar attendance.
Food and Drug Administration
Center for Devices and Radiological Health
Center for Devices and Radiological Health
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