Cart Summary
0 item(s) ($0.00)
Product Categories
Schedule of Events

TitleCityState/ ProvinceDate Registration
PV0820Process Validation for Medical Devices - VirtualVirtual Attendance Only Aug 10, 2020
RM0820Integrating Risk Management into the Product Life CycleVirtual Attendance Only Aug 18, 2020
QSIH090720The Quality System Regulation 21 CFR 820 and ANSI/AAMI/ISO 13485: Navigating Regulatory RequirementsVirtual Attendance Only Sep 07, 2020
DCIH092120Design Control Requirements - Integrating The Quality System Regulation and ANSI AAMI ISO 13485Virtual Attendance Only Sep 21, 2020
QS0920The Quality System Regulation 21 CFR 820 and ANSI/AAMI/ISO 13485: Navigating Regulatory RequirementsVirtual Only-USA EST Sep 21, 2020
PVIH092820Process Validation and Industry Requirements for a Global MarketVirtual Attendance Only Sep 28, 2020
DC0920Design Control Requirements • Integrating the Quality System Regulation and ANSI/AAMI/ISO 13485Virtual Only-USA EST Sep 30, 2020
RMIH101220Integrating Risk Management into the Product Life CycleVirtual Attendance Only Oct 12, 2020
QS1120The Quality System Regulation 21 CFR 820 and ANSI/AAMI/ISO 13485: Navigating Regulatory RequirementsArlingtonVANov 02, 2020
RM1120Integrating Risk Management into the Product Life CycleArlingtonVANov 17, 2020
DC1220Design Control Requirements • Integrating the Quality System Regulation and ANSI/AAMI/ISO 13485ArlingtonVADec 15, 2020