Medical Devices
-
?
-
Workshops & Conferences (Medical Devices)
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 which take place after October 1, 2011.
#Includes presentations
-
Current Medical Device Meetings and Workshops
Public Workshop - ASTM-FDA Workshop on Absorbable Medical Devices: Lessons Learned from Correlations of Bench Testing and Clinical Performance, November 28, 2012 - FDA's Clinical Investigator Training Course, November 13-15, 2012
- 2012 RAPS: The Regulatory Convergence, October 26-30, 2012
Public Workshop - FDA/American Glaucoma Society Workshop on the Validity, Reliability, and Usability of Glaucoma Imaging Devices, October 5, 2012 AAMI/FDA Interoperability Summit, October 2-3, 2012 Public Workshop - Medical Countermeasures (MCM) for a Burn Mass Casualty Incident, September 27-28, 2012 Public Meeting - Regulatory Science Considerations for Medical Countermeasure Radiation Biodosimetry Devices, September 27-28, 2012 HHS Federal Research Update on Lyme Disease Diagnostics Activities, September 24, 2012 FDA Small Business Regulatory Education for Industry (REdI) Conference Fall 2012, September 19-20, 2012 - Public Workshop - Leveraging Registries With Medical Device Data for Postmarket Surveillance and Evidence Appraisal Throughout the Total Product Life Cycle, September 12-13, 2012
- Public Workshop - MDEpiNet 2012 Annual Meeting: The Medical Device Epidemiology Network as a Partnership for Building Global Medical Device Epidemiology and Surveillance Capabilities, September 11, 2012
- Public Meeting - Strengthening the National Medical Device Postmarket Surveillance System, September 10, 2012
Public Workshop - Post Approval Studies 2012 Workshop: Design, Methodology, and Role in Evidence Appraisal throughout the Total Product Life Cycle, August 30, 2012 Public Workshop - Division of Cardiovascular (DCD) 30-Day Notices and Annual Reports Workshop, August 28, 2012 Public Workshop - Device Improvements for Pediatric X-ray Imaging, July 16, 2012 Public Meeting - Clinical Study Design and Performance of Hospital Glucose Sensors, June 25, 2012 Educational Forum on MDR, Complaints, and Recalls, Corrections, and Removals, June 15, 2012 15th Annual FDA-OCRA Educational Conference, June 6-7, 2012 FDA/Xavier University Medical Device Conference, May 1-4, 2012 - The Food and Drug Law Institute's (FDLI) 55th Annual Conference, April 24-25, 2012
Association of Medical Diagnostics Manufacturers (AMDM) 39th Annual Meeting & OIVD Submissions Workshop, April 17-20, 2012 Public Workshop - Medical Device User Fee Program Public Meeting, March 28, 2012 Public Workshop - Cardiovascular Metallic Implants: Corrosion, Surface Characterization, and Nickel Leaching, March 8-9, 2012 Public Workshop - Design and Methodology for Postmarket Surveillance Studies under Section 522 of the Federal Food, Drug and Cosmetic Act, March 7, 2012 Public Workshop - Using Scientific Research Data to Support Pediatric Medical Device Claims, December 5, 2011 Public Workshop - Bridging the IDEAL and TPLC Approaches for Evidence Development for Surgical Medical Devices and Procedures, December 2, 2011 - Patient-Centeredness in Policy and Practice - ECRI Institute's 18th Annual Conference Co-sponsored by U.S. Food and Drug Administration, November 29-30, 2011
- Public Workshop - Magnetic Resonance Imaging Safety, October 25-26, 2011
2011 RAPS: The Regulatory Convergence, October 22-26, 2011 Public Meeting - Advancing Regulatory Science for Highly Multiplexed Microbiology/MCM Devices, October 13, 2011# - AdvaMed 2011 - The MedTech Conference, September 26-28, 2011#
- Two-day Tissue Adhesives / Soft Tissue Workshop / Symposium, September 26-27, 2011
Town Hall Discussion With the Director of CDRH and Other Senior Center Management, September 22, 2011 2011 PDA/FDA Joint Regulatory Conference, September 19-21, 2011 - Public Meeting - Recommendations Proposed in Institute of Medicine Report: "Medical Devices and the Public’s Health, The FDA 510(k) Clearance Process at 35 Years," September 16, 2011
Center for Devices and Radiological Health Forum for International Medical Device Regulatory Authorities (Advanced Session), September 13-16, 2011 - Public Workshop - Mobile Medical Applications Draft Guidance, September 12-13, 2011#
- Unique Device Identification (UDI) for Postmarket Surveillance and Enforcement Public Workshop, September 12-13, 2011#
- FDA / NHLBI/ NSF Workshop on Computer Methods for Medical Devices: Validation of Computer with Nonclinical Models, September 7-9, 2011
-
-
-