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Schedule of Events

TitleCityState/ ProvinceDate Registration
HWHT190521WEBINAR: HTM Best Practices in Large Health Systems  May 21, 2019
HWHT190523Webinar: Using HTM Data to Drive High Reliability Healthcare  May 23, 2019
STEQ1906EQ - Medical Equipment Management Committee MeetingClevelandOHJun 06, 2019
AC19AAMI Exchange 2019ClevelandOHJun 07, 2019
HALE0619HTM Annual Leadership Exchange (HALE)ClevelandOHJun 07, 2019
AEM190607AEM Workshop - Cleveland, OHClevelandOHJun 07, 2019
STSM051906AAMI SM-WG05 Device Security Working GroupArlingtonVAJun 10, 2019
STRD1906AAMI/ID, Infusion Devices CommitteeArlingtonVAJun 11, 2019
STSM031906AAMI SM-WG03, Interoperability Working Group MeetingArlingtonVAJun 12, 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
STWG121907July 2019 ST/WG 84 and ST/WG 12 Interim MeetingsArlingtonVAJul 08, 2019
STCN011907AAMI CN/WG 01, Luer activated valves MeetingArlingtonVAJul 09, 2019
HWHT190716WEBINAR: Monthly Workload Tracker by Technician Using Data Modeling  Jul 16, 2019
RM0819Integrating Risk Management into the Product Life Cycle - July 2019ArlingtonVAJul 30, 2019
HWCE190820Webinar: Maximizing the Value of ACI Certification and Understanding Recertification Requirements  Aug 20, 2019
EO0819Industrial Ethylene Oxide Sterilization for Medical Devices Workshop - August 2019ArlingtonVAAug 27, 2019
QSIH090919AAMI/CQT Solutions The Quality System Regulation 21 CFR 820 and ANSI/AAMI/ISO 13485: Navigating Regulatory Requirements- September 2019 IrelandDublin Sep 09, 2019
HF0919Human Factors for Medical Devices - September 2019ArlingtonVASep 10, 2019
HFIH091619AAMI/CQT Human Factors for Medical Devices - IrelandDublin Sep 16, 2019
QS0919The Quality System Regulation 21 CFR 820 and ANSI/AAMI/ISO 13485: Navigating Regulatory Requirements-September 2019ArlingtonVASep 16, 2019
AP0919Effective Application of Agile Practices in the Development of Medical Device Software - September 2019ArlingtonVASep 23, 2019
DC0919Design Control Requirements • Integrating the Quality System Regulation and ANSI/AAMI/ISO 13485 - September 2019ArlingtonVASep 24, 2019
AA0919The Application of Agile to the Development of Medical Device Systems - September 2019ArlingtonVASep 25, 2019
DCIH093019AAMI/CQT Solutions Design Control Requirements - Integrating The Quality System Regulation and ANSI AAMI ISO 13485Dublin Sep 30, 2019
IS1019Industrial Sterilization for Medical Devices - October 2019ArlingtonVAOct 01, 2019
PV1019Process Validation for Medical Devices: Requirements and Standards - October 2019ArlingtonVAOct 08, 2019
ST1941910ISO/TC194/WG15 Ad hoc MeetingArlingtonVAOct 17, 2019
QS1019The Quality System Regulation 21 CFR 820 and ANSI/AAMI/ISO 13485: Navigating Regulatory Requirements- October 2019ArlingtonVAOct 28, 2019
ST19421910ISO/TC194/WG2 Ad hoc MeetingArlingtonVAOct 28, 2019
RS1119Radiation Sterilization for Medical Devices - November 2019ArlingtonVANov 05, 2019
RM1119Integrating Risk Management into the Product Life Cycle - November 2019ArlingtonVANov 13, 2019
HF1119Human Factors for Medical Devices - November 2019ArlingtonVANov 19, 2019
QS1219The Quality System Regulation 21 CFR 820 and ANSI/AAMI/ISO 13485: Navigating Regulatory Requirements- December 2019ArlingtonVADec 09, 2019
DC1219Design Control Requirements • Integrating the Quality System Regulation and ANSI/AAMI/ISO 13485 - December 2019ArlingtonVADec 10, 2019