This page provides information on meetings, workshops, and other events that include CDRH participation, including FDA presentations for FDA sponsored and FDA Co-Sponsored meetings in 2016.
List of Meetings and Workshops
FDA/Patient Workshop (By Invitation Only) - The Intersection of Regulatory Science and Patient Experience, August 1, 2016
- Public Workshop - Liquid Biopsies in Oncology Drug and Device Development, An FDA-AACR public workshop, July 19, 2016
Workshop - 9th Annual Medical Device and Diagnostics Statistical Issues, Co-Sponsored by AdvaMed and FDA, May 3-4, 2016 Public Workshop - Mass Spectrometry in the Clinic: Regulatory Considerations Surrounding Validation of Liquid Chromatography-Mass Spectrometry Based Devices, May 2, 2016 Public Workshop - Streamlining Good Manufacturing Practices (GMPs) for Hearing Aids, April 21, 2016 CDRH Industry Basics Workshop - Unique Device Identification (UDI) Part II, Submitting Information to GUDID, March 10th, 2016 Public Workshop - Point of Care Prothrombin Time/International Normalized Ratio Devices for Monitoring Warfarin Therapy, March 18, 2016 (New Date) Public Workshop - Patient and Medical Professional Perspectives on the Return of Genetic Test Results, March 2, 2016 Public Workshop - Next Generation Sequencing-Based Oncology Panels, February 25, 2016 CDRH Industry Basics Workshop - Unique Device Identification (UDI), January 27, 2016 Public Workshop - Moving Forward: Collaborative Approaches to Medical Device Cybersecurity, January 20-21, 2016