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MDMA's PMA 510(k) Workshop & FDA Forum
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MDMA's PMA 510(k) Workshop & FDA Forum

Join us at MDMA’s popular TWO day FDA Forum on March 16-17, 2016 in Palo Alto, CA. This conference will focus on unique insights and strategies to govern the 510(k) and PMA regulatory pathways. This is a great way for companies considering submitting a 510(k) or PMA to get the tools they need to prepare successful submissions.

3/16/2016 to 3/17/2016
When: March 16-17, 2016
Where: Crowne Plaza Cabana Hotel
4290 El Camino Real
Palo Alto 94306
United States
Contact: Sheri DeVinney
202-354-7171

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Join us at MDMA’s popular TWO day FDA Forum on March 16-17, 2016 in Palo Alto, CA.  This conference will focus on unique insights and strategies to govern the 510(k) and PMA regulatory pathways. This is a great way for companies considering submitting a 510(k) or PMA to get the tools they need to prepare successful submissions.

Topics Include:
Navigating Today’s 510(k) Program
Clinical Trial Considerations
The Growing De Novo Program
Do’s & Don’ts of Pre-Submission Meetings
PMA Review Considerations
MDUFA III Update & Looking Ahead to MDUFA IV
Best Practices When Interacting with FDA
Key Post Market Intiative

We also have a great panel of industry experts for the interactive session, "Applying Lessons Learned/Case Studies.”

MDMA Members - $695
FMMC Members - $795 
Non-Members - $895

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