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Schedule of Events

TitleCityState/ ProvinceDate Registration
QS1019The Quality System Regulation 21 CFR 820 and ANSI/AAMI/ISO 13485: Navigating Regulatory RequirementsArlingtonVAOct 28, 2019
RM1119Integrating Risk Management into the Product Life CycleArlingtonVANov 13, 2019
QS1219The Quality System Regulation 21 CFR 820 and ANSI/AAMI/ISO 13485: Navigating Regulatory RequirementsArlingtonVADec 09, 2019
DC1219Design Control Requirements • Integrating the Quality System Regulation and ANSI/AAMI/ISO 13485ArlingtonVADec 10, 2019
DC0120Design Control Requirements • Integrating the Quality System Regulation and ANSI/AAMI/ISO 13485ArlingtonVAJan 28, 2020
QS0220The Quality System Regulation 21 CFR 820 and ANSI/AAMI/ISO 13485: Navigating Regulatory RequirementsArlingtonVAFeb 10, 2020
RM0320Integrating Risk Management into the Product Life CycleArlingtonVAMar 10, 2020
DC0320Design Control Requirements • Integrating the Quality System Regulation and ANSI/AAMI/ISO 13485ArlingtonVAMar 24, 2020
PV0420Process Validation for Medical Devices: Requirements and StandardsArlingtonVAApr 14, 2020
QS0420The Quality System Regulation 21 CFR 820 and ANSI/AAMI/ISO 13485: Navigating Regulatory RequirementsArlingtonVAApr 27, 2020
CP0620Corrective and Preventive Action Requirements and Industry PracticeArlingtonVAJun 02, 2020