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Schedule of Events

TitleCityState/ ProvinceDate Registration
ITAF1118Industry Training Advisory Forum  Nov 29, 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 MeetingTORINOITALYDec 03, 2018
STSW1812Standards Week December 2018ArlingtonVADec 03, 2018
ITCAF1218Corporate Member Industry Training Advisory Forum  Dec 06, 2018
DCD18Design Control-Integrating The Quality System Regulation and ANSI/AAMI/ISO 13485 RequirementsArlingtonVADec 10, 2018
GMD18The Quality System Regulation 21 CFR 820 and ANSI/AAMI/ISO 13485: Navigating Regulatory RequirementsArlingtonVADec 10, 2018
STWDPDP - Device ParticulatesArlingtonVADec 12, 2018
STSP1901AAMI SP - Sphygmomanometer Working Group MeetingArlingtonVAJan 07, 2019
STWG841901AAMI ST/WG 84 Interim Meeting, January 2019ArlingtonVAJan 08, 2019
HF0119Human Factors for Medical Devices - January 2019ArlingtonVAJan 23, 2019
STID1901AAMI ID - Infusion Devices Working Group MeetingArlingtonVAJan 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
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
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
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-Junel 2019ArlingtonVAJun 24, 2019