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Schedule of Events

TitleCityState/ ProvinceDate Registration
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
RM03192Integrating Risk Management into the Product Lifecycle: Quality and 13485 - March 2019ArlingtonVAMar 12, 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 for Medical Devices: Requirements and Standards - April 2019ArlingtonVAApr 16, 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
RM0819Integrating Risk Management into the Product Lifecycle: Quality and 13485 - August 2019ArlingtonVAAug 27, 2019
QS0919The Quality System Regulation 21 CFR 820 and ANSI/AAMI/ISO 13485: Navigating Regulatory Requirements-September 2019ArlingtonVASep 16, 2019
DC0919Design Control Requirements • Integrating the Quality System Regulation and ANSI/AAMI/ISO 13485 - September 2019ArlingtonVASep 24, 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