MDMA 2013 FDA Forum
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3/14/2013 to 3/15/2013
When: 3/14/2013
Where: Crowne Plaza Cabana Hotel
4290 El Camino Real
Palo Alto, California  94306
United States
Contact: Sheri DeVinney

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MDMA's popular TWO day seminar will focus on unique insights and strategies to govern 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. Presentations will be made by leading FDA officials, industry representatives and policy experts.

This Seminar Will Cover:

  • Navigating Today's 510(k) Program
  • PMA Review Considerations
  • Changing Landscape at FDA, an Industry Perspective
  • Key Post-Market Initiatives
  • Adapting to FDA's Newest Guidance Documents

The program will provide valuable insight from a variety of perspectives and give companies considering submitting a 510(k) or PMA in the future the tools they need to prepare successful submissions.

Click here to view agenda