| 2008 |
Sep 22-26
San Diego, CA |
Quality System Requirements and Industry Practice |
Sep 30
Webinar |
Design Transfer: Best Practices for the Successful Transfer of Medical Devices from Research and Development to Manufacturing  |
Oct 1-3
Arlington, VA |
Integrating Risk Management into the Quality System |
Oct 8
Webinar |
Validation of Software for Regulated Processes: An Overview of AAMI TIR36: 2007 |
Oct 13-16
Arlington, VA |
Industrial Sterilization for Medical Devices |
Oct 14
Webinar |
Changes to Your Quality Management System: Planning for Unpredictable Consequences |
Oct 16
Webinar |
Water Quality for Reprocessing of Medical Devices: A Review of Key Aspects of the New AAMI TIR34 |
Oct 20-22
Arlington, VA |
Industrial Ethylene Oxide Sterilization for Medical Devices |
Oct 20-24
London, UK |
Quality System Requirements and Industry Practice |
Oct 27-29
Phoenix, AZ |
Process Validation Requirements and Industry Practice |
Nov 3-5
San Diego, CA |
Building a Quality Management System in a Regulated Environment: A 13485 Workshop |
Nov 3-5
Las Vegas, NV |
Software Validation Requirements and Industry Practice |
Nov 10-13
Arlington, VA |
Radiation Sterilization for Medical Devices |
Dec 1-3
San Diego, CA |
Design Control Requirements and Industry Practice |
Dec 8-12
Arlington, VA |
Quality System Requirements and Industry Practice |
| 2009 |
Jun 6 – 8
Baltimore, MD |
2009 Annual Conference and Expo: Call for Proposals
2009 Annual Conference and Expo |
| 2010 |
Jun 26 – 28
Tampa, FL |
2010 Annual Conference and Expo |
