| 2009 |
Sep 7-11
Brussels, Belgium |
Quality System Requirements and Industry Practice |
Sep 14-16
Phoenix, AZ |
Industrial Ethylene Oxide Sterilization for Medical Devices Workshop |
Sep 16-18
San Francisco, CA |
Design Control Requirements and Industry Practice |
Sep 21-24
Dallas, TX |
Industrial Sterilization for Medical Devices |
Sep 21-25
Minneapolis, MN |
Quality System Requirements and Industry Practice |
Sep 22
Webinar |
Introduction to Statistical Methods and Tools for a Quality System |
Sep 30-Oct 2
Arlington, VA |
Human Factors for Medical Devices  |
Oct 5-7
Arlington, VA |
Software Validation Requirements and Industry Practice |
Oct 12-14
Arlington, VA |
Building a Quality Management System in a Regulated Environment: A 13485 Workshop |
Oct 19-21
San Francisco, CA |
Integrating Risk Management into the Quality System  |
Oct 26-30
Las Vegas, NV |
Quality System Requirements and Industry Practice |
Nov 2-4
Arlington, VA |
Process Validation Requirements and Industry Practice |
Nov 9-11
Arlington, VA |
Design Control Requirements and Industry Practice |
Nov 16-18
Philadelphia, PA |
Document Control and Records Management for Medical Devices |
Dec 7-11
Arlington, VA |
Quality System Requirements and Industry Practice |
| 2010 |
Jun 26 – 28
Tampa, FL |
2010 AAMI Annual Conference and Expo: Call for Proposals |
