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Schedule of Events

TitleCityState/ ProvinceDate Registration
ISCQMS0620ISC Online Session: The Future of Quality Management Systems  Jun 08, 2020
HWHT20609HTM Live!: Getting the CMMS to Work for Us  Jun 09, 2020
STEQEX2006AAMI EQ - Medical Equipment Management Meeting - **POSTPONEDNew OrleansLAJun 10, 2020
ISCRM0620ISC Online: Future of Risk Management for Medical Technology  Jun 10, 2020
ISCPMS0620ISC Online Session: Post-Market Surveillance  Jun 12, 2020
ISCDHI0620ISC Online Session: The FDA's Digital Health Initiative  Jun 15, 2020
SLSCY0620AAMI Summer Learning Series: Cybersecurity Track  Jun 15, 2020
ISCCMT0620ISC Online Session: Cybersecurity and Medical Technologies  Jun 17, 2020
ISCSW0620ISC Online Session: Software  Jun 19, 2020
SLSHTM0620AAMI Summer Learning Series: HTM Track  Jun 19, 2020
QS0620The Quality System Regulation 21 CFR 820 and ANSI/AAMI/ISO 13485: Navigating Regulatory RequirementsVirtual Attendance Only Jun 22, 2020
ISCHIT0620ISC Online Session: Health Software and Health IT Systems  Jun 22, 2020
ISCAI0620ISC Online Session: Artificial Intelligence  Jun 24, 2020
STHE2004AAMI HE - Human Factors Engineering Co. Meeting *NEW DATE*  Jun 25, 2020
SLSREG0720AAMI Summer Learning Series: Regulatory/Accreditation Track  Jul 10, 2020
AP0720Effective Application of Agile Practices in the Development of Medical Device SoftwareVirtual Attendance Only Jul 14, 2020
SLSPRO0720AAMI Summer Learning Series: Professional Development Track  Jul 22, 2020
SLSAR0720AAMI Summer Learning Series: AI-AR/VR Track  Jul 27, 2020
PV0820Process Validation for Medical Devices - VirtualVirtual Attendance Only Aug 10, 2020
SLSSTR0820AAMI Summer Learning Series: Sterilization Track  Aug 10, 2020
HWHT200811HTMLive!: Understanding the Stages of ACI Certification  Aug 11, 2020
RM0820Integrating Risk Management into the Product Life CycleArlingtonVAAug 18, 2020
SLSIOT0820AAMI Summer Learning Series: IoT Track  Aug 21, 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 RequirementsVirtual Attendance Only Sep 07, 2020
HWHT0920HTMLive!: Protecting & Maintaining Medical Devices  Sep 08, 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 13485Virtual Attendance Only Sep 21, 2020
PVIH092820Process Validation and Industry Requirements for a Global MarketVirtual Attendance Only Sep 28, 2020
DC0920Design Control Requirements • Integrating the Quality System Regulation and ANSI/AAMI/ISO 13485ArlingtonVASep 30, 2020
IS1020Industrial Sterilization for Medical DevicesArlingtonVAOct 06, 2020
SVIH101220Medical Device Software ValidationDun LaoghaireDublinOct 12, 2020
RS1020Radiation Sterilization for Medical DevicesArlingtonVAOct 27, 2020
QS1120The Quality System Regulation 21 CFR 820 and ANSI/AAMI/ISO 13485: Navigating Regulatory RequirementsArlingtonVANov 02, 2020
RM1120Integrating Risk Management into the Product Life CycleArlingtonVANov 17, 2020
HF1220Human Factors for Medical DevicesArlingtonVADec 01, 2020
DC1220Design Control Requirements • Integrating the Quality System Regulation and ANSI/AAMI/ISO 13485ArlingtonVADec 15, 2020