| 2010 |
February 1-5
Arlington, VA |
Statistical Methods and Tools for a Quality System |
February 15-19
Arlington, VA |
Quality System Requirements and Industry Practice |
February 24
Webinar |
ISO 80369 Small Bore Connectors Standards: Implications for Clinical Users, Manufacturers, and Component Suppliers  |
March 9 - 10
Reston, VA |
AAMI/FDA International Conference on Medical Device Standards and Regulation |
March 15-17
Arlington, VA |
Process Validation Requirements and Industry Practice |
March 18
Webinar |
Effective Risk-Based CAPA Investigations Based on the New GHTF Guidance Document  |
March 24
Webinar |
Overview on the new AAMI/IEC 80002-1 Medical Device Software Risk Management Technical Report  |
March 24-26
Arlington, VA |
Design Control Requirements and Industry Practice |
April 7-9
Boston, MA |
Software Validation Requirements and Industry Practice |
April 13-15
New Orleans, LA |
Document Control and Records Management for Medical Devices |
April 19-21
Arlington, VA |
Human Factors for Medical Devices |
April 26-30
San Francisco, CA |
Quality System Requirements and Industry Practice |
May 10-12
Arlington, VA |
Corrective and Preventive Action Requirements and Industry Practice |
May 11-14
Minneapolis, MN |
Industrial Sterilization for Medical Devices |
May 24-26
New Orleans, LA |
Design Control Requirements and Industry Practice |
June 7-9
Arlington, VA |
Purchasing Controls and Supply Chain Management  |
June 14-18
Orlando, FL |
Quality System Requirements and Industry Practice |
June 21-23
Arlington, VA |
Integrating Risk Management into the Quality System |
June 26–28
Tampa, FL |
2010 AAMI Annual Conference and Expo |
September 13-17
Arlington, VA |
Quality System Requirements and Industry Practice |
Sept 27 - Oct 1
Las Vegas, NV |
Statistical Methods and Tools for a Quality System |
October 4-6
Atlanta, GA |
Industrial Ethylene Oxide Sterilization for Medical Devices Workshop |
October 11-13
Arlington, VA |
Software Validation Requirements and Industry Practice |
October 18-20
Minneapolis, MN |
Human Factors for Medical Devices |
October 18-22
Galway, Ireland |
Quality System Requirements and Industry Practice |
October 25-27
Phoenix, AZ |
Document Control and Records Management for Medical Devices |
November 1-5
Coronado, CA |
Quality System Requirements and Industry Practice |
November 3-5
Coronado, CA |
Process Validation Requirements and Industry Practice |
November 8-10
Coronado, CA |
Design Control Requirements and Industry Practice |
November 8-10
Coronado, CA |
Integrating Risk Management into the Quality System |
December 7-9
Phoenix, AZ |
Purchasing Controls and Supply Chain Management  |
December 7-10
Phoenix, AZ |
Radiation Sterilization for Medical Devices |
| 2011 |
Jun 25-27
San Antonio, TX
|
2011 AAMI Annual Conference and Expo |