• Medical Device Manufacturers Association's 2018 FDA Forum

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    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:
    • 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
    Location:
    Crowne Plaza Cabana Hotel
    4290 El Camino Real
    Palo Alto, California  94301-3842
    Date/Time Information:
    March 12-13, 2018
    Contact Information:
    Sheri DeVinney
    Fees/Admission:
    Online registration is available until March 13. NCBIO Members receive a $100 discount. 

    MDMA Member Rate: $595
    Non-Member Rate: $895

     
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