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- Draft Guidance: FDA Categorization of Investigational Device Exemption (IDE) Devices to Assist the Centers for Medicaid Services (CMS) with Coverage Decisions
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.
To hear the presentation and ask questions: 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/
cc/events_vbc1/join?id= PW9026935&role=attend&pw= pk8pXK%3DnG
Following the webinar, a transcript, recording and slides will be available at: http://www.fda.gov/CDRHWebinar
. The slide presentation will also be available on this page on the morning of the webinar.
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