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Schedule of Events

TitleCityState/ ProvinceDate Registration
DC0120Design Control Requirements • Integrating the Quality System Regulation and ANSI/AAMI/ISO 13485ArlingtonVAJan 28, 2020
HWHT200130Webinar: Health Technology Alliance Webinar: Cybersecurity - The New Norm for HTM  Jan 30, 2020
STCP20011AAMI CP - Combination Products Committee MeetingArlingtonVAJan 31, 2020
HF0220Human Factors for Medical DevicesArlingtonVAFeb 04, 2020
QS0220The Quality System Regulation 21 CFR 820 and ANSI/AAMI/ISO 13485: Navigating Regulatory RequirementsArlingtonVAFeb 10, 2020
HWHT200211HTM LIVE! (Webinar): Hospital Margins Hit 10-Year Low: How to reduce operational time and cost through an asset retirement plan  Feb 11, 2020
STBE2002AAMI BE - Biological Evaluation Committee MeetingArlingtonVAFeb 18, 2020
STHIT2002Joint Meetings of the AAMI Health IT CommitteeArlingtonVAFeb 18, 2020
STSM012002AAMI SM-WG01, Software Working Group MeetingArlingtonVAFeb 19, 2020
HFIH030220Human Factors for Medical DevicesCambridge, United Kingdom Mar 02, 2020
ST62MT2003IEC/SC 62D/MT 20 - Haemodialysis equipmentArlingtonVAMar 02, 2020
ST1502001ISO/TC 150/SC 6/JWG 2 MeetingArlingtonVAMar 04, 2020
RMIH030920Integrating Risk Management into the Product Life CycleDun Laoghaire Dublin Ireland Mar 09, 2020
RM0320Integrating Risk Management into the Product Life CycleArlingtonVAMar 10, 2020
HWHT200310HTMLive! (Webinar) The Use of Analytics in Healthcare Technology Management  Mar 10, 2020
STWSP2003March 2020 Sterilization Standards WeekArlingtonVAMar 16, 2020
QSIH032320The Quality System Regulation 21 CFR 820 and ANSI/AAMI/ISO 13485: Navigating Regulatory RequirementsFreising Germany Mar 23, 2020
DCIH032320Design Control Requirements - Integrating The Quality System Regulation and ANSI AAMI ISO 13485Freising Germany Mar 23, 2020
DC0320Design Control Requirements • Integrating the Quality System Regulation and ANSI/AAMI/ISO 13485ArlingtonVAMar 24, 2020
ST62PT2004IEC/SC 62A/Project Team Meeting for 60601-4-5ArlingtonVAApr 06, 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 2020ArlingtonVAApr 20, 2020
ST62CG2004IEC/SC 62A/AG 33, Chairman's Advisory Group MeetingArlingtonVAApr 23, 2020
QS0420The Quality System Regulation 21 CFR 820 and ANSI/AAMI/ISO 13485: Navigating Regulatory RequirementsArlingtonVAApr 27, 2020
STWG202004IEC/SC 62A/WG 20 - Environmental Protection MeetingArlingtonVAApr 27, 2020
STHE2004AAMI HE - Human Factors Engineering Committee MeetingArlingtonVAApr 28, 2020
HF0520Human Factors for Medical DevicesArlingtonVAMay 05, 2020
IS0520Industrial Sterilization for Medical DevicesArlingtonVAMay 12, 2020
CP0620Corrective and Preventive Action Requirements and Industry PracticeArlingtonVAJun 01, 2020
PC0620Purchasing Controls and Supply Chain ManagementArlingtonVAJun 03, 2020
ST62JG2006IEC/SC 62D - ISO/TC 173/JWG 4 - Medical Beds MeetingArlingtonVAJun 08, 2020
AC20AAMI Exchange 2020New OrleansLAJun 12, 2020
QS0620The Quality System Regulation 21 CFR 820 and ANSI/AAMI/ISO 13485: Navigating Regulatory RequirementsArlingtonVAJun 22, 2020
AP0720Effective Application of Agile Practices in the Development of Medical Device SoftwareArlingtonVAJul 14, 2020
HFM0720Human Factors MethodologiesArlingtonVAJul 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
QSIH090720AAMI/CQT Solutions The 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
DCIH092120AAMI/CQT Solutions Design Control Requirements - Integrating The Quality System Regulation and ANSI AAMI ISO 13485Dun LaoghaireDublinSep 21, 2020
PVIH092820AAMI/CQT Solutions Process 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
RMIH101220AAMI/CQT Risk ManagementDun LaoghaireDublinOct 12, 2020
SVIH101220AAMI/CQT Medical 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