Medical Device Manufacturers Association's 2018 FDA Forum
Name:
Medical Device Manufacturers Association's 2018 FDA Forum
Date:
March 12, 2018 - March 13, 2018
Event Description:
MDMA’s 2018 FDA Forum continues to grow as the conference to engage with leading policy makers and experts. This popular two day seminar focuses on unique insights and strategies to navigate the 510(k) and PMA regulatory pathways.
Confirmed FDA Speakers Include:
Confirmed FDA Speakers Include:
- William Maisel, Deputy Center Director for Science & Chief Scientist, CDRH, FDA
- Sean Boyd, Deputy Director for Regulatory Affairs, Office of Compliance, FDA
- Abiy Desta, Ombudsman, CDRH, FDA (via video conferencing)
- Elizabeth Hillebrenner, Associate Director for Programs and Performance, Office of In Vitro Diagnostics and Radiological Health, CDRH, FDA
- Joshua Nipper, Chief of Premarket Approval Staff, Office of Device Evaluation, CDRH, FDA
- Bakul Patel, Associate Director for Digital Health, Office of the Center Director, CDRH, FDA
- Marjorie Shulman, Chief of Premarket Notification (510(k)) Section, Office of Device Evaluation, CDRH, FDA
- Suzanne Schwartz, MD, MBA, Associate Director for Science and Strategic Partners hips, Office of the Center Director, CDRH, FDA
