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AAMI Individual Membership
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Schedule of Events

TitleCityState/ ProvinceDate Registration
HF0119Human Factors for Medical Devices - January 2019ArlingtonVAJan 23, 2019
AEM0119AEM TrainingIndianapolisINJan 25, 2019
STID1901AAMI ID - Infusion Devices Working Group MeetingArlingtonVAJan 29, 2019
HWHT190129WEBINAR: Part 1 - Developing an HTM Specific Cybersecurity Framework  Jan 29, 2019
DC0119Design Control-Integrating The Quality System Regulation and ANSI/AAMI/ISO 13485 Requirements - January 2019ArlingtonVAJan 30, 2019
QS0219The Quality System Regulation 21 CFR 820 and ANSI/AAMI/ISO 13485: Navigating Regulatory Requirements-February 2019ArlingtonVAFeb 04, 2019
HWHT190205WEBINAR: Part 2 - Developing an HTM Specific Cybersecurity Framework  Feb 05, 2019
HWHT190219WEBINAR: Bluetooth in the Healthcare Setting  Feb 19, 2019
RM03192Integrating Risk Management into the Product Lifecycle: Quality and 13485 - March 2019ArlingtonVAMar 12, 2019
STCV1903AAMI CV - Cardiac Valve Prostheses Committee MeetingNew OrleansLAMar 12, 2019
HWHT190313WEBINAR: Using LinkedIn to Market Yourself and Your Organization  Mar 13, 2019
DC0319Design Control Requirements • Integrating the Quality System Regulation and ANSI/AAMI/ISO 13485 - March 2019ArlingtonVAMar 26, 2019
QS0419The Quality System Regulation 21 CFR 820 and ANSI/AAMI/ISO 13485: Navigating Regulatory Requirements-April 2019ArlingtonVAApr 08, 2019
PV04192Process Validation Requirements and Industry Practice-April 2019ArlingtonVAApr 16, 2019
STLAVC1904AAMI CN/WG 01 - Luer Activated Valves Committee MeetingArlingtonVAApr 16, 2019
HWHT190416WEBINAR: Part 3 - Developing an HTM Specific Cybersecurity Framework  Apr 16, 2019
STDP1904AAMI DP - Medical Device Particulates Committee MeetingArlingtonVAApr 17, 2019
ISC2019AAMI/BSI/FDA International Standards Conference - April 2019RestonVAApr 24, 2019
HF0419Human Factors for Medical Devices - April 2019ArlingtonVAApr 30, 2019
SV0519Regulatory Requirements for Software ValidationArlingtonVAMay 07, 2019
SVW0519Software Validation Workshop: Practical Tools and TechniquesArlingtonVAMay 07, 2019
IS0519Industrial Sterilization for Medical Devices - May 2019ArlingtonVAMay 14, 2019
AC19AAMI Exchange 2019ClevelandOHJun 07, 2019
CP0619Corrective and Preventive Action Requirements and Industry Practice-June 2019ArlingtonVAJun 18, 2019
PC0619Purchasing Controls & Supply Chain Management-June 2019ArlingtonVAJun 19, 2019
QS0619The Quality System Regulation 21 CFR 820 and ANSI/AAMI/ISO 13485: Navigating Regulatory Requirements-June 2019ArlingtonVAJun 24, 2019
HWHT190716WEBINAR: Monthly Workload Tracker by Technician Using Data Modeling  Jul 16, 2019
RM0819Integrating Risk Management into the Product Lifecycle: Quality and 13485 - August 2019ArlingtonVAJul 30, 2019
EO0819Ethylene Oxide Sterilization for Medical Devices - Aug 2019ArlingtonVAAug 27, 2019
HF0919Human Factors for Medical Devices - September 2019ArlingtonVASep 10, 2019
QS0919The Quality System Regulation 21 CFR 820 and ANSI/AAMI/ISO 13485: Navigating Regulatory Requirements-September 2019ArlingtonVASep 16, 2019
AP0919Effective Application of Agile Practices in the Development of Medical Device Software - September 2019ArlingtonVASep 23, 2019
DC0919Design Control Requirements • Integrating the Quality System Regulation and ANSI/AAMI/ISO 13485 - September 2019ArlingtonVASep 24, 2019
AA0919The Application of Agile to the Development of Medical Device Systems - September 2019ArlingtonVASep 25, 2019
IS1019Industrial Sterilization for Medical Devices - October 2019ArlingtonVAOct 01, 2019
PV1019Process Validation for Medical Devices: Requirements and Standards - October 2019ArlingtonVAOct 08, 2019
QS1019The Quality System Regulation 21 CFR 820 and ANSI/AAMI/ISO 13485: Navigating Regulatory Requirements- October 2019ArlingtonVAOct 28, 2019
RS1119Radiation Sterilization for Medical Devices - November 2019ArlingtonVANov 05, 2019
RM1119Integrating Risk Management into the Product Lifecycle: Quality and 13485 - November 2019ArlingtonVANov 13, 2019
HF1119Human Factors for Medical Devices - November 2019ArlingtonVANov 19, 2019
QS1219The Quality System Regulation 21 CFR 820 and ANSI/AAMI/ISO 13485: Navigating Regulatory Requirements- December 2019ArlingtonVADec 09, 2019
DC1219Design Control Requirements • Integrating the Quality System Regulation and ANSI/AAMI/ISO 13485 - December 2019ArlingtonVADec 10, 2019