Past CDRH Workshops & Meetings

• National Registry on Safety & Atrial Fibrillation Ablation: An Incubator Thinktank, April 27-28, 2009 
• FDA Unique Device Identification Public Workshop: February 12, 2009 
• FDA/AAO/AAO/AOA/CLAO Workshop: Microbiological Testing for Contact Lens Care Products, January 22-23, 2009 
• FDA/AdvaMed Workshop: Gender Differences in Cardiovascular Device Trials, December 9, 2008 
• FDA Workshop: Best Practices For Pacemaker and ICD Lead Postmarket Surveillance, October 2-3, 2008 
• FDA Workshop: Exploration of Public Policy Development Regarding the Study and Analysis of Sex Differences in the Clinical Evaluation of Cardiovascular Medical Products, June 2, 2008 
• AMDM/FDA - OIVD 510(k) Workshop - April 22-23, 2008 
• FDA / NHLBI / NSF Workshop on Computer Methods for Cardiovascular Devices, March 18-19, 2008 
• AMDM/FDA - OIVD 510(k) Workshop - April 17-18, 2007 
• Risk Communication on Medical Devices: Sharing Perspectives - Sept. 26, 2006  
• AMDM/FDA– OIVD 510(k) WORKSHOP - April 18-19, 2006 
• FDA Workshop on Regulatory Process for Pediatric Mechanical Circulatory Support Devices (Ventricular Assist Devices), January 20, 2006 
• AMDM/FDA - OIVD 510(k) WORKSHOP - April 19-20, 2005 
• 2004 FDA Workshop on Pre-Clinical Testing for Endovascular Grafts - July 28 - 29, 2004 
• FDA Workshop: IVD Roundtable 510(k) Workshop - April 22-23, 2003  
• Proceedings from the Workshop on Preclinical Testing for Endovascular Grafts - July 31 - August 1, 2001 
• Radiological Health Reengineering Workshop - November 15-16, 2000 
• The Role of Clinical Data in Postmarket Surveillance of Cardiovascular Devices - Workshop Summary - February 2-3, 2000