Join
Events
2019
August
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August 20 Webinar: Maximizing the Value of ACI Certification and Understanding Recertification Requirements
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August 27 – 30 Industrial Ethylene Oxide Sterilization for Medical Devices Workshop - August 2019
Arlington, VA
September
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September 9 – 13 The Quality System Regulation 21 CFR 820 and ANSI/AAMI/ISO 13485: Navigating Regulatory Requirements- September 2019 Ireland
Dublin
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September 10 U.S. TAG to ISO/TC210 Meeting
Arlington, VA
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September 10 – 12 Human Factors for Medical Devices - September 2019
Arlington, VA
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September 16 – 20 The Quality System Regulation 21 CFR 820 and ANSI/AAMI/ISO 13485: Navigating Regulatory Requirements-September 2019
Arlington, VA
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September 16 – 18 AAMI/CQT Human Factors for Medical Devices - Ireland
Dublin
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September 17 Webinar: From HTM To C-Suite
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September 23 – 24 Effective Application of Agile Practices in the Development of Medical Device Software - September 2019
Arlington, VA
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September 24 – 26 Design Control - September 2019
Arlington, VA
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September 25 – 27 Agile Systems - September 2019
Arlington, VA
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September 30 – October 2 AAMI/CQT Design Control Requirements
Dublin
October
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October 1 – 4 Industrial Sterilization for Medical Devices - October 2019
Arlington, VA
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October 8 – 10 Process Validation - October 2019
Arlington, VA
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October 17 ISO/TC194/WG15 Ad hoc Meeting
Arlington, VA
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October 28 – 29 ISO/TC194/WG2 TR 37137-2 Writing group Meeting
Arlington, VA
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October 28 – November 1 Quality System - October 2019
Arlington, VA
November
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November 5 – 8 Radiation Sterilization for Medical Devices - November 2019
Arlington, VA
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November 6 – 7 AAMI DP- Medical Device Particulates Committee Meeting
Arlington, VA
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November 13 – 15 Risk Management - November 2019
Arlington, VA
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November 19 – 21 Human Factors for Medical Devices - November 2019
Arlington, VA