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Schedule of Events

TitleCityState/ ProvinceDate Registration
DCCQTMY18Design Control Requirements and Industry PracticeDun Laoghaire, Dublin, Ireland May 28, 2018
AC18AAMI 2018 Conference & ExpoLong BeachCAJun 01, 2018
HTMLA0618HTM Leadership AcademyLong BeachCAJun 04, 2018
STWSUM1806Summer Standards Week - June 4-8, 2018Long BeachCAJun 04, 2018
CPJN18Corrective and Preventive Action Requirements and Industry PracticeArlingtonVAJun 12, 2018
GMJN18The Quality System Regulation 21 CFR 820 and ANSI/AAMI/ISO 13485: Navigating Regulatory RequirementsArlingtonVAJun 18, 2018
ISC0618AAMI/BSI International Conference on Medical Device Standards and Regulations (European Conference)London (Heathrow), UK Jun 19, 2018
HFCQTJN18Human Factors for Medical Devices CourseManchester England UK Jun 26, 2018
WBHT180710Webinar: HTM Leadership Online Certificate Program  Jul 10, 2018
WBSU1807RRWebinar: Best Practices in Reprocessing Reusable Medical Devices  Jul 17, 2018
STINTS1807AAMI ST/WG 84 Interim Meeting, July 2018ArlingtonVAJul 19, 2018
GMITRI0718The Quality System Regulation 21 CFR 820 and ANSI/AAMI/ISO 13485: Navigating Regulatory RequirementsHsinchu Jul 23, 2018
WBHT1803UDWebinar: The Benefits of UDI for Healthcare Technology Management  Jul 31, 2018
WBSU1808ENWebinar: Processing Flexible Endoscopes: Current Evidence-Based Guidelines  Aug 22, 2018
EOAG18Ethylene Oxide Sterilization for Medical Devices CourseArlingtonVAAug 28, 2018
DCAG18Design Control Requirements & Industry Practice CourseArlingtonVAAug 29, 2018
DCCQTS18Design Control Requirements and Industry Practice85354 Freising, Germany Sep 05, 2018
RMITRI0918Integrating Risk Management Into the Quality SystemHsinchu Sep 10, 2018
DCITRI0918Design Control Requirements and Industry PracticeHsinchu Sep 12, 2018
HFS18Human Factors for Medical Devices CourseArlingtonVASep 17, 2018
AAS18The Application of Agile to the Development of Medical Device SystemsArlingtonVASep 19, 2018
GMS18The Quality System Regulation 21 CFR 820 and ANSI/AAMI/ISO 13485: Navigating Regulatory RequirementsArlingtonVASep 24, 2018
GMCQTO18The Quality System Regulation 21 CFR 820 and ANSI/AAMI/ISO 13485: Navigating Regulatory RequirementsDun Laoghaire, Dublin Oct 01, 2018
APO18Effective Application of Agile Practices in the Development of Medical Device SoftwareLas VegasNVOct 15, 2018
HFCQTO18Human Factors for Medical DevicesDun Laoghaire, Dublin Oct 15, 2018
RSO18Radiation Sterilization for Medical DevicesArlingtonVAOct 16, 2018
SVTTO18Software Validation Workshop: Practical Tools & TechniquesLas VegasNVOct 17, 2018
PVO18Process Validation Requirements and Industry PracticeArlingtonVAOct 24, 2018
GMCQTD18The Quality System Regulation 21 CFR 820 and ANSI/AAMI/ISO 13485: Navigating Regulatory RequirementsManchester England Dec 03, 2018
ISCQTD18Industrial Sterilization for Medical DevicesManchester England Dec 03, 2018