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Schedule of Events

TitleCityState/ ProvinceDate Registration
HWHT200330AAMI and IAHCSMM Joint Webinar: Sterilization and COVID-19  Mar 30, 2020
CBETSC0420CBET Study Course  Apr 06, 2020
PV0420Process Validation and Industry Requirements for a Global MarketArlingtonVAApr 14, 2020
HWHT200414HTM Live! (Webinar): Learn how HTM professionals can improve patient safety by helping to reduce alarm fatigue in healthcare settings  Apr 14, 2020
ISC2020International Standards Conference 2020 *CANCELED*ArlingtonVAApr 20, 2020
QS0420The Quality System Regulation 21 CFR 820 and ANSI/AAMI/ISO 13485: Navigating Regulatory RequirementsArlingtonVAApr 27, 2020
STHE2004AAMI HE - Human Factors Engineering Comm. Meeting *REMOTE*ArlingtonVAApr 28, 2020
STRD2005AAMI RD - Renal Disease and Detoxification Meeting *REMOTE*ArlingtonVAMay 04, 2020
HF0520Human Factors for Medical DevicesArlingtonVAMay 05, 2020
IS0520Industrial Sterilization for Medical DevicesArlingtonVAMay 12, 2020
510K05202Navigating 510(k) & De Novo RequirementsArlingtonVAMay 18, 2020
HWHT200519HTMLive! Webinar: Precision Healthcare and the Internet of Things  May 19, 2020
HWHT200521HTM Live! (Webinar) Medical Devices on Your Network: Assessing and Understanding the Risks  May 21, 2020
CP0620Corrective and Preventive Action Requirements and Industry PracticeArlingtonVAJun 01, 2020
PC0620Purchasing Controls and Supply Chain ManagementArlingtonVAJun 03, 2020
STDP2006AAMI DP - Medical Device Particulates Committee MeetingArlingtonVAJun 04, 2020
STEQEX2006AAMI EQ - Medical Equipment Management Committee MeetingNew OrleansLAJun 10, 2020
AC20AAMI Exchange 2020New OrleansLAJun 12, 2020
QS0620The Quality System Regulation 21 CFR 820 and ANSI/AAMI/ISO 13485: Navigating Regulatory RequirementsArlingtonVAJun 22, 2020
SV0620Production & Quality System SoftwareArlingtonVAJun 23, 2020
AP0720Effective Application of Agile Practices in the Development of Medical Device SoftwareArlingtonVAJul 14, 2020
QS0720The Quality System Regulation 21 CFR 820 and ANSI/AAMI/ISO 13485: Navigating Regulatory RequirementsLas VegasNVJul 20, 2020
DC0720Design Control Requirements • Integrating the Quality System Regulation and ANSI/AAMI/ISO 13485Las VegasNVJul 21, 2020
RM0820Integrating Risk Management into the Product Life CycleArlingtonVAAug 18, 2020
EO0820Ethylene Oxide Sterilization for Medical DevicesArlingtonVAAug 25, 2020
HF0920Human Factors for Medical DevicesArlingtonVASep 01, 2020
QSIH090720The Quality System Regulation 21 CFR 820 and ANSI/AAMI/ISO 13485: Navigating Regulatory RequirementsDun LaoghaireDublinSep 07, 2020
SV0920Medical Device Software ValidationArlingtonVASep 09, 2020
QS0920The Quality System Regulation 21 CFR 820 and ANSI/AAMI/ISO 13485: Navigating Regulatory RequirementsArlingtonVASep 21, 2020
HFIH092120Human Factors for Medical DevicesDun LaoghaireDublinSep 21, 2020
DCIH092120Design Control Requirements - Integrating The Quality System Regulation and ANSI AAMI ISO 13485Dun LaoghaireDublinSep 21, 2020
PVIH092820Process Validation and Industry Requirements for a Global MarketDun LaoghaireDublinSep 28, 2020
DC0920Design Control Requirements • Integrating the Quality System Regulation and ANSI/AAMI/ISO 13485ArlingtonVASep 30, 2020
IS1020Industrial Sterilization for Medical DevicesArlingtonVAOct 06, 2020
RMIH101220Integrating Risk Management into the Product Life CycleDun LaoghaireDublinOct 12, 2020
SVIH101220Medical Device Software ValidationDun LaoghaireDublinOct 12, 2020
RS1020Radiation Sterilization for Medical DevicesArlingtonVAOct 27, 2020
QS1120Quality System November 2020ArlingtonVANov 02, 2020
RM1120Risk Management - November 2020ArlingtonVANov 17, 2020
HF1220Human Factors for Medical DevicesArlingtonVADec 01, 2020
DC1220Design Control - December 2020ArlingtonVADec 15, 2020