This page provides information on public events that include CDRH participation which may be of educational value to the general medical device community.
A Tour of the FDA -- A web-based course providing basic information about FDA along with quizzes to test your knowledge. The course was developed under a Cooperative Research and Development Agreement between FDA and EduNeering, Inc.
SCHEDULE FOR WORKSHOPS WITH CDRH PARTICIPATION
Date |
Event/Location |
Lead CDRH Office |
|---|---|---|
April 2009 |
||
| April 21-22 | AMDM/FDA - OIVD 510(k) Workshop | OIVD |
June 2009 |
||
| June 8-9 | AFDO/FDA; Drugs and Devices--Promoting and Protecting the Public Health Through Risk Management and Product Cycle Improvement; Chicago, IL | OC/OSB |
| June 8-11 | MD&M East; New York, NY | OCER/OC |
DSMICA - Division of Small Manufacturers, International and Consumer Assistance
OC - Office of Compliance
OCD - Office of the Center Director
ODE - Office of Device Evaluation
OCER - Office of Communication, Education, and Radiation Programs (Formerly OHIP)
OIVD - Office of In Vitro Diagnostics
ORA - Office of Regulatory Affairs
OSB - Office of Surveillance and Biometrics
OSEL - Office of Science and Engineering Laboratories (formerly OST)
For more information on these workshops contact the appropriate cooperating organization listed below:
| Organization |
Phone |
|---|---|
| AAMI - Association for the Advancement of Medical Instrumentation | 703-525-4890 ext.203 |
| AdvaMed - Advanced Medical Technology Association | 202-783-8700 |
| AMDM - Association of Medical Diagnostic Manufacturers | 202-637-6837 |
| ASQ - American Society for Quality | 800-248-1946 |
|
|
| FDLI - Food, Drug, and Law Institute | 202-371-1420 |
| MDM - Medical Design and Manufacturing Conference | 310-445-4200 |
| OCRA (Orange County Regulatory Affairs) Discussion Group | 949-222-9022 |
| RAPS - Regulatory Affairs Professionals Society | 301-770-2920 |
Updated April 1, 2009
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