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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
(September 2004
through September 2005)
October
2004; November
2004; December 2004; January 2005;
February 2005; March 2005;
April 2005; May 2005; June 2005; July
2005; August 2005; September 2005
Date |
Event/Location |
Lead CDRH Office |
---|---|---|
October 10-13 | RAPS 2004 Annual Conference & Exhibition, Washington, DC |
ODE/OC/OSB
|
October 26-27 |
Premarket Notification 510(k)
Reviewer Training for Third Party Organizations, Gaithersburg, MD, |
ODE/DSMICA
|
October 26-27 | AdvaMed: The Use of Standards in Submissions, Alexandria, VA |
ODE/OSEL/OC
|
November 10 | AdvaMed Audio Conference: Recall Classification and Public Notification |
OC
|
January 10-12 | MDM West, Anaheim, CA |
DSMICA
|
April 4-7 | AAMI, Quality System Requirements and Industry Practice, Galway, Ireland |
OC
|
May 16-19 | AAMI, Quality System Requirements and Industry Practice, Miami, FL |
OC
|
June 13-15 | AAMI, Design Control Requirements & Industry Practice, Washington, DC |
OC
|
Sep 19-22 | AAMI, Quality System Requirements and Industry Practice, San Antonio, TX |
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 Device Manufacturers | 202-637-6837 |
ASQ - American Society for Quality | |
800-492-6961 |
|
- Biomedical Focus/St. Paul |
612-545-1919 |
- Customer Supplier Div. |
800-645-6707 |
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 November 4, 2004
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