![]() ![]() ![]() ![]() |
FDA
Home Page | CDRH Home Page | Search
| CDRH
A-Z Index | Contact CDRH
|
CDRH Presentations |
Title | Date | Formats | ||
---|---|---|---|---|
Improving the Availability of Pediatric Devices - American Academy of Pediatrics - Washington DC | 6/28/04 | Text | ||
FDLI Conference: FDA Regulation of Genomic and Genetic Diagnostic Devices | 4/16/04 | PPT | Text | |
FDLI Conference: Device Issues | 4/16/04 | PPT | Text | |
FDLI Conference: The Division of Bioresearch Monitoring Case Studies | 4/16/04 | PPT | Text | |
FDLI Conference: EPA/FDA Regulatory Partnerships and Partitions | 4/16/04 | PPT | Text | |
FDLI Conference: Custom Devices | 4/16/04 | PPT | Text | |
FDLI Conference: Ombudsman | 4/16/04 | PPT | Text | |
AdvaMed Submissions Workshop - Medical Devices: Innovation
and Regulation |
6/5/03 | PPT | Text | |
FDA's CLIA Complexity Process | 4/23/02 | PPT | Text | |
Estimated Benefits of Proposed Amendments to the FDA Radiation-Safety Standard for Diagnostic X-Ray Equipment | 12/31/01 | PPT | Text | |
Evaluating Breakthrough Technology: An FDA Perspective | 06/15/2001 | PPT | Text | |
CLIA Update: June 5, 2001 | 06/05/2001 | PPT | ||
FDA's Final Policy on Single-Use Devices Reprocessed by Hospitals and Commercial Reprocessors | 05/10/2001 05/30/2001 |
PPT | Text | |
MDMA Presentation - CDRH: Looking Ahead | 05/18/2001 | PPT | ||
FDLI Presentation: Closing Gaps in Our Postmarket Safety Net for Medical Devices: It’s Everybody’s Business! | 04/18/2001 | PPT | Text | |
FDLI Presentation: CDRH - Looking Ahead | 04/18/2001 | PPT | ||
Estimated Benefits of Proposed Amendments to the FDA Radiation-Safety Standard for Diagnostic X-Ray Equipment | 02/15-16/2001 | PPT | Text | |
Gaps in Your Postmarket Safety Net for Medical Devices | 1/8/2001 | PPT | Text | |
CDRH Executive Briefing - RAPS Annual Meeting | 10/2000 | PPT | ||
Device Regulation in an International Milieu | 9/25/2000 | PPT | ||
Polyvinyl Chloride and DEHP | 9/20/2000 | PPT | ||
Global Challenges in Human Factors and Medical Systems Mini-symposia | 8/2/2000 | PPT | ||
CDRH Overview | 7/18/2000 | PPT | ||
Future Trends | 7/19/2000 | PPT | ||
Role of the CDRH Ombudsman | 7/2000 | PPT | ||
The FDA Modernization Act | 6/29/2000 | PPT | ||
CDRH Update - MDMA | 6/12/2000 | PPT | ||
AAMI 2000 Conference and Expo | 6/6/2000 | PPT | ||
CDRH Update - FDLI | 6/5/2000 | PPT | ||
FDA and the Reuse of Single Use Devices: Policy Moving Forward - FASA Presentation | 5/6/2000 | PPT | ||
Staff Update: The Least Burdensome Provisions of FDAMA | 4/2/2000 | PPT | ||
CDRH: Moving Forward | 3/23/2000 | PPT | ||
The Role of Standards at CDRH | 3/15/2000 | PPT | ||
Patient Safety: Emerging Opportunities in the Health Care System | 3/2000 | PPT | ||
Statement By David W. Feigal, M.D. Director, CDRH, Before The Subcommittee On Oversight And Investigations Committee On Commerce U.S. House Of Representatives | 2/10/2000 | Text | ||
Part 11 News and Views - Electronic Records and Electronic Signatures Regulation | 1/13/2000 | PPT | ||
CDRH Update | 12/16/1999 | PPT | ||
The Least Burdensome Provisions of the FDA Modernization Act of 1997 - Training for CDRH Advisory Panels | 12/99 | PPT | ||
The Least Burdensome Provisions of the FDA Modernization Act of 1997 | 12/13/1999 | PPT | ||
CDRH Top Priorities 2000 | 12/10/1999 | PPT | ||
Standards of Evidence for Drug Approvals | 12/9/1999 | PPT | ||
Assessment of the Quality of Life Impact of Medical Devices | 11/4/1999 | PPT | ||
Current Issues for Medical Devices | 11/2/1999 | PPT | ||
Pharmacogenomics: A regulatory perspective | 10/28/1999 | PPT | ||
Least Burdensome Pathway to Market | 10/25/1999 | PPT | ||
Protein PK/PD A Regulatory Perspective | 10/19/1999 | PPT | ||
Current Issues for Medical Devices in the U.S. | 10/12/1999 | PPT | ||
CDRH Executive Briefing | 10/4/1999 | PPT | ||
CDRH Update | 9/27/1999 | PPT | ||
QSIT Corrective and Preventive Actions | various | PPT | ||
QSIT: Design Controls and Production and Process Controls | various | PPT | ||
QSIT Management Controls | various | PPT | ||
The Quality System Inspection Technique: QSIT | various | PPT | ||
QSIT: Compliance Program and Warning Letter Pilot | various | PPT | ||
Dispute Resolution at CDRH | 7/27/1999 | PPT | ||
CDRH Directions | 7/27/1999 | PPT | ||
FDLI Medical Device Update | 6/29/1999 | PPT | ||
Medical Device User Fees | 5/25/1999 | PPT |
CDRH Home Page | CDRH A-Z Index | Contact CDRH | Accessibility | Disclaimer
FDA Home Page | Search FDA Site | FDA A-Z Index | Contact FDA | HHS Home Page
Center for Devices and Radiological Health / CDRH