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Breakout

Breakout #1: CDRH Premarket Update

Thursday, April 23, 2026
1:30 PM - 3:00 PM East Coast USA Time
Location: Franklin AB - 2nd Floor

    Moderator(s)

  • Heather Rosecrans

    Executive Vice President, Medical Devices & Combination Products
    MDMA & ELIQUENT Life Sciences

  • Bill Brodbeck

    Vice President, Regulatory Affairs
    STERIS Corporation

    • Speaker(s)

  • Clarence Murray, III

    Director, Regulatory Affairs
    STERIS Corporation

  • Josh Nipper

    Director, PreMarket Operations, Office of Product Evaluation and Quality (OPEQ), Center for Devices and Radiological Health (CDRH)
    FDA

    View Slides

  • Mike Ryan

    Executive VP, Medical Devices and Combination Products
    Eliquent Life Sciences

Hear from FDA leaders regarding medical device premarket submission pathways, best practices and new initiatives. Learn about submission trends and premarket program highlights that can help you determine the best path to ensure your device gets to the patients that need it in the most efficient and timely manner.