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MDMA's FDA Forum: PMA/510(k) Workshop
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MDMA's FDA Forum: PMA/510(k) Workshop

3/14/2019 to 3/15/2019
When: March 14-15, 2018
Where: Crowne Plaza Cabana Hotel
4250 El Camino Real
Palo Alto 94306
United States
Contact: Sheri DeVinney
202-354-7171

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Have you ever left a conference and realized that you forgot to ask the question you came to get answered?  Ever wonder what the FDA’s criteria may be when reviewing your PMA/510(k) submission? Join us at MDMA’s FDA Forum on March 14-15, 2019 in Palo Alto, CA to get your questions answered. MDMA’s 2019 FDA Forum continues to grow as THE conference to engage with leading policy makers and experts. Be sure not to miss out hearing from FDA officials on how to get your technologies into the marketplace.

 

Confirmed FDA Speakers Include:

 

·       William Maisel, Deputy Center Director for Science & Chief Scientist, CDRH, FDA

·       Sergio M. de del Castillo, De Novo Program Lead, Office of Device Evaluation, CDRH, FDA

·       Joshua Nipper, Director, PMA, HDE, & Q-Sub Programs, Program Operations Staff, Office of Device Evaluation, CDRH, FDA

·       Kathryn M. O’Callaghan, Assistant Director for Strategic Programs, Office of the Center Director, 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

·       Timothy Stenzel, MD, PhD, Director, Office of In Vitro Diagnostics and Radiological Health, CDRH, FDA

·       Michelle Tarver, Director, Patient Science & Engagement Program, Office of the Center Director, CDRH, FDA

 

This is a RARE opportunity to share YOUR concerns and ask YOUR questions from some of the FDA's top officials.

 

MDMA Members - $595

State Member - $795

Non-Members - $895

 

FMMC members enter the promotional code: STATE to receive your $100 discount

 

For more information and to register, CLICK HERE

 

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