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Schedule of Events

TitleCityState/ ProvinceDate Registration
GMS18The Quality System Regulation 21 CFR 820 and ANSI/AAMI/ISO 13485: Navigating Regulatory RequirementsArlingtonVASep 24, 2018
GMCQTO18The Quality System Regulation 21 CFR 820 and ANSI/AAMI/ISO 13485: Navigating Regulatory RequirementsDun Laoghaire, Dublin Oct 01, 2018
STBE11ST63Joint Meeting of AAMI BE/WG 11 and ST/WG 63  Oct 10, 2018
APO18Effective Application of Agile Practices in the Development of Medical Device SoftwareLas VegasNVOct 15, 2018
HFCQTO18Human Factors for Medical DevicesDun Laoghaire, Dublin Oct 15, 2018
RSO18Radiation Sterilization for Medical DevicesArlingtonVAOct 16, 2018
SVTTO18Software Validation Workshop: Practical Tools & TechniquesLas VegasNVOct 17, 2018
STWFA1810Fall Sterilization Standards Week - October 22-25, 2018BaltimoreMDOct 22, 2018
PVO18Process Validation Requirements and Industry PracticeArlingtonVAOct 24, 2018
GMO18The Quality System Regulation 21 CFR 820 and ANSI/AAMI/ISO 13485: Navigating Regulatory RequirementsArlingtonVAOct 29, 2018
HFN18Human Factors for Medical Devices CourseArlingtonVANov 06, 2018
RMN18Integrating Risk Management into the Product Lifecycle: Quality and 13485ArlingtonVANov 07, 2018
ISCQTD18Industrial Sterilization for Medical DevicesManchester England Dec 03, 2018
GMCQTD18The Quality System Regulation 21 CFR 820 and ANSI/AAMI/ISO 13485: Navigating Regulatory RequirementsManchester England Dec 03, 2018
STCNIT1812AAMI/CN/WG 01, Luer Activated Valves MeetingTORINO Dec 03, 2018
GMD18The Quality System Regulation 21 CFR 820 and ANSI/AAMI/ISO 13485: Navigating Regulatory RequirementsArlingtonVADec 10, 2018
DCD18Design Control-Integrating The Quality System Regulation and ANSI/AAMI/ISO 13485 RequirementsArlingtonVADec 10, 2018
HF0119Human Factors for Medical Devices - January 2019ArlingtonVAJan 23, 2019