Medical Devices
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Past Workshops & Conferences
This page provides information on past meetings, workshops, and other public events that included CDRH participation.
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2011
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Device Regulatory Authorities (Advanced Session), September 13-16, 2011 Public Workshop - Mobile Medical Applications Draft Guidance, September 12-13, 2011 Unique Device Identification (UDI) for Postmarket Surveillance and Compliance Public Workshop, September 12-13, 2011 FDA / NHLBI / NSF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 Ultra High Throughput Sequencing for Clinical Diagnostic Applications - Approaches to Assess Analytical Validity, June 23, 2011 Public Workshop - Reprocessing of Reusable Medical Devices, June 8-9, 2011 FDA Workshop - Seizure Detection, Cognitive Function, and TBI/Concussion Devices: Issues in Their Evaluation, June 2-3, 2011 Public Workshop - Study Methodologies for Diagnostics in the Postmarket Setting, May 12, 2011 Town Hall Discussion With the Director of CDRH and Other Senior Center Management, May 5, 2011 Center for Devices and Radiological Health Forum for International Medical Device Regulatory Authorities, May 3-6, 2011 510(k) Implementation: Discussion of an On-line Repository of Medical Device Labeling, and of Making Device Photographs Available in a Public Database Without Disclosing Proprietary Information, April 7, 2011 Public Workshop - Center for Devices and Radiological Health's Innovation Initiative, March 15, 2011 Town Hall Discussion With the Director of CDRH and Other Senior Center Management, March 10, 2011
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2010
FDA Public Workshop on External Defibrillators, December 15-16, 2010 Public Workshop - Innovations in Technology for the Treatment of Diabetes: Clinical Development of the Artificial Pancreas (an Autonomous System), November 10, 2010 2010 mHealth Summit on Mobile Technologies in Health Research and Policy, November 8-10, 2010
Medical Devices Technology Innovation Partnership (MD-TIP) Workshop, October 26, 2010 Town Hall Discussion With the Director of CDRH and Other Senior Center Management, October 7, 2010 AAMI and FDA Summit on Infusion Devices, Oct. 5-6, 2010
Public Workshop - Optimizing Clinical Trial Design for the Development of Pediatric Cardiovascular Devices, September 30th, 2010 Public Workshop - Medical Devices and Nanotechnology: Manufacturing, Characterization, and Biocompatibility Considerations, September 23, 2010 Public Workshop: Medical Device User Fee Program Public Meeting, September 14, 2010 Public Workshop - ASK CHILDREN (Assess Specific Kinds of CHILDREN Challenges for Neurologic Devices) STUDY Workshop, September 13, 2010 2010 PDA/FDA Joint Regulatory Conference, September 13-16, 2010
CDRH Forum for International Medical Device Regulatory Authorities - Advanced Session, September 13-15, 2010 Public Meeting: Converged Communications and Health Care Devices Impact on Regulation, July 26-27, 2010 FDA/CDRH Public Meeting: Oversight of Laboratory Developed Tests (LDTs), Date July 19-20, 2010 Array-Based Cytogenetic Tests: Questions on Performance Evaluation, Result Reporting and Interpretation, June 30, 2010 Public Hearing: Development of Articles for Rare Diseases, June 29-30, 2010 Public Workshop: Identifying Unmet Public Health Needs and Facilitating Innovation in Medical Device Development, June 24, 2010 Town Hall Discussion With the Director of CDRH and Other Senior Center Management, June 22, 2010 13th Annual FDA-OCRA Educational Conference, June 16 & 17, 2010 Drug Information Association 46th Annual Meeting, June 13-17, 2010
FDA / NHLBI / NSF Workshop on Computer Methods for Cardiovascular Devices, June 10-11, 2010: The integration of nonclinical and computer models Public Meeting - Device Improvements to Reduce the Number of Under-Doses, Over-Doses, and Misaligned Exposures From Therapeutic Radiation, June 9-10, 2010 Medical Design & Manufacturing (MD&M) East Conference, June 7-10, 2010
Public Meeting: Infusion Pump Workshop, May 25-26, 2010 Medical Device Use in the Home Environment Workshop: Implications for the Safe and Effective Use of Medical Device Technology Migrating Into the Home, May 24, 2010 Town Hall Discussion With the Director of CDRH and Other Senior Center Management, May 18, 2010 CDRH Forum for International Medical Device Regulatory Authorities, May 3-6, 2010 Public Meeting: Device Improvements to Reduce Unnecessary Radiation Exposure from Medical Imaging, March 30-31, 2010 Pediatric Assessments of Neurological and Neurocognitive Function for Cardiovascular Devices Workshop, March 25, 2010 FDA/CDRH Public Meeting: Blood Glucose Meters - March 16-17, 2010 PMA Submissions Workshop, February 25-26, 2010
Investigational Device Exemption (IDE) Submission Workshop, February 24, 2010
510(k) Submissions - The Course for Beginning RA Professionals for Preparing a 510(k), Feburary 22-23, 2010
Public Meeting: Strengthening the Center for Devices and Radiological Health’s 510(k) Review Process, February 18, 2010 Public Meeting: Incorporation of New Science Into Regulatory Decisionmaking Within the Center for Devices and Radiological Health - February 9, 2010 The A to Z of Off Label Issues, February 9, 2010
Medical Device Interoperability, January 25, 2010 Thermal Aspects of Radio Frequency Exposure, January 11-12, 2010
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2009
FDA-IDSA Public Workshop: Advancing Clinical Development of Molecular and Other Diagnostic Tests for Respiratory Tract Infections, November 12-13, 2009 FDA Pediatric Clinical Trials Workshop: Unmet Needs, Trial Designs and Clinically Meaningful Safety and Effectiveness Outcomes, October 29-30, 2009 2009 PDA/FDA Joint Regulatory Conference, September 14-18, 2009
Center for Devices and Radiological Health Forum for International Medical Device Regulatory Authorities, September 14-16, 2009 FDA Workshop: Methodologies for Post-Approval Studies of Medical Devices, September 9-10, 2009 Introduction to Medical Device Research and Making the Risk Determination, June 17, 2009 FDA Workshop: Implementation of Post Approval Studies for Medical Devices, June 4-5, 2009 FDA / NHLBI / NSF Workshop on Computer Methods for Cardiovascular Devices, June 1-2, 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
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2008
2008 FDA Critical Path Workshop: Clinical Trials for Local Treatment of Breast Cancer by Thermal Ablation 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
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2007-2003
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
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