This two day seminar focuses on insights and strategies to navigate the 510(k) and PMA regulatory pathways, as well as what changes to expect with the implementation of the user fee reauthorization and FDA reforms.
Connfirmed FDA Speakers Include:
-William Maisel, Deputy Center Director for Science & Chief Scientist, CDRH, FDA,
- Thinh Nguyen, Director, Office of Combination Products, FDA,
- Bakul Patel, Associate Director for Digital Health, Office of Center Director, CDRH, FDA,
- John Sheets, Director, Office of Devices, CDRH, FDA, - Murray Sheldon, Associate Director for Technology and Innovation, CDRH, FDA,
- John Weiner, Associate Director for Policy & Product Classification Officer, Office of Combination Products, FDA
Crowne Plaza Cabana Hotel
Palo Alto, California
http://www.medicaldevices.org/events/EventDetails.aspx?id=886687
Wednesday, March 08, 2017 to Thursday, March 09, 2017