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Schedule of Events

TitleCityState/ ProvinceDate Registration
HF1119Human Factors for Medical DevicesArlingtonVANov 19, 2019
HWHT191121Webinar: HTM in a Box Orientation  Nov 21, 2019
STSM051912AAMI SM-WG05, Device Security Working Group MeetingArlingtonVADec 02, 2019
STCSS1912CSS/Standards Board - December 3rd 2019ArlingtonVADec 03, 2019
STWV1912AAMI WV - Waveform Testing Committee MeetingArlingtonVADec 03, 2019
STDSW1912AAMI ID - Infusion Device Committee MeetingArlingtonVADec 04, 2019
STECG1912AAMI EC - ECG Committee MeetingArlingtonVADec 04, 2019
STSM031912AAMI SM-WG03, Interoperability Working Group MeetingArlingtonVADec 04, 2019
STPC1912AAMI PC - Cardiac Rhythm Device Management Committee MeetingArlingtonVADec 05, 2019
STDF1912AAMI DF - Defibrillator Committee MeetingArlingtonVADec 05, 2019
STCPRO1912AAMI CP - Combination Products Committee MeetingArlingtonVADec 06, 2019
QS1219The Quality System Regulation 21 CFR 820 and ANSI/AAMI/ISO 13485: Navigating Regulatory RequirementsArlingtonVADec 09, 2019
DC1219Design Control Requirements • Integrating the Quality System Regulation and ANSI/AAMI/ISO 13485ArlingtonVADec 10, 2019
STSM1910AAMI SM - Software and Information Technology CommitteeArlingtonVADec 10, 2019
HWHT191217Webinar: Stepping Through the New Environment on Imaging QA and TJC Requirements  Dec 17, 2019
EO1020Ethylene Oxide Sterilization for Medical DevicesArlingtonVAJan 14, 2020
HWHT200114Building Cybersecurity into the Medical Device Lifecycle  Jan 14, 2020
STMT232001IEC/SC 62D/MT 23 - Infusion Pumps MeetingArlingtonVAJan 21, 2020
DC0120Design Control Requirements • Integrating the Quality System Regulation and ANSI/AAMI/ISO 13485ArlingtonVAJan 28, 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
RM0320Integrating Risk Management into the Product Life CycleArlingtonVAMar 10, 2020
DC0320Design Control Requirements • Integrating the Quality System Regulation and ANSI/AAMI/ISO 13485ArlingtonVAMar 24, 2020
PV0420Process Validation for Medical Devices: Requirements and StandardsArlingtonVAApr 14, 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
HF0520Human Factors for Medical DevicesArlingtonVAMay 05, 2020
IS0520Industrial Sterilization for Medical DevicesArlingtonVAMay 12, 2020
CP0620Corrective and Preventive Action Requirements and Industry PracticeArlingtonVAJun 02, 2020