Join
Events
2019
December
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December 9 – 13 The Quality System Regulation 21 CFR 820 and ANSI/AAMI/ISO 13485: Navigating Regulatory Requirements
Arlington, VA
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December 10 AAMI SM - Software and Information Technology Committee
Arlington, VA
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December 10 – 12 Design Control Requirements – Integrating the Quality System Regulation and ANSI/AAMI/ISO 13485
Arlington, VA
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December 17 HTM LIVE! (Webinar): Stepping Through the New Environment on Imaging QA and TJC Requirements
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December 19 Webinar: There’s a new version of MDS2 in town!
2020
January
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January 14 – 17 Ethylene Oxide Sterilization for Medical Devices
Arlington, VA
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January 14 HTM LIVE! (Webinar): Building Cybersecurity into the Medical Device Lifecycle
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January 21 – 24 IEC/SC 62D/MT 23 - Infusion Pumps Meeting
Arlington, VA
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January 28 – 30 Design Control Requirements – Integrating the Quality System Regulation and ANSI/AAMI/ISO 13485
Arlington, VA
February
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February 4 – 6 Human Factors for Medical Devices
Arlington, VA
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February 10 – 14 The Quality System Regulation 21 CFR 820 and ANSI/AAMI/ISO 13485: Navigating Regulatory Requirements
Arlington, VA
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February 11 Hospital Margins Hit 10-Year Low: How To Reduce Operational
March
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March 2 – 4 AAMI/CQT Solutions Human Factors for Medical Devices
Cambridge, United Kingdom
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March 9 – 11 AAMI/CQT Solutions Integrating Risk Management into the Product Life Cycle
Dun Laoghaire Dublin
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March 10 – 12 Integrating Risk Management into the Product Life Cycle
Arlington, VA
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March 23 – 25 AAMI/CQT Solutions Design Control Requirements - Integrating The Quality System Regulation and ANSI AAMI ISO 13485
Munich Germany
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March 23 – 27 AAMI/CQT Solutions The Quality System Regulation 21 CFR 820 and ANSI/AAMI/ISO 13485: Navigating Regulatory Requirements
Munich Germany
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March 24 – 26 Design Control Requirements – Integrating the Quality System Regulation and ANSI/AAMI/ISO 13485
Arlington, VA
April
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April 14 HTM Live! (Webinar): Learn how HTM professionals can improve
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April 14 – 16 Process Validation for Medical Devices: Requirements and Standards
Arlington, VA
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April 23 – 24 IEC/SC 62A/AG 33, Chairman's Advisory Group Meeting
Arlington, VA
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April 27 – 28 IEC/SC 62A/WG 20 - Environmental Protection Meeting
Arlington, VA
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April 27 – May 1 The Quality System Regulation 21 CFR 820 and ANSI/AAMI/ISO 13485: Navigating Regulatory Requirements
Arlington, VA
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April 28 – 30 AAMI HE - Human Factors Engineering Committee Meeting
Arlington, VA
May
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May 5 – 7 Human Factors for Medical Devices
Arlington, VA
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May 12 – 15 Industrial Sterilization for Medical Devices
Arlington, VA
June
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June 2 – 3 Risk Management and Human Factors
Arlington, VA
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June 2 – 3 Corrective and Preventive Action Requirements and Industry Practice
Arlington, VA
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June 3 – 5 Purchasing Controls and Supply Chain Management
Arlington, VA
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June 12 – 15 AAMI Exchange 2020
New Orleans, LA
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June 22 – 26 The Quality System Regulation 21 CFR 820 and ANSI/AAMI/ISO 13485: Navigating Regulatory Requirements
Arlington, VA
July
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July 14 – 15 Effective Application of Agile Practices in the Development of Medical Device Software
Arlington, VA
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July 14 – 15 Human Factors Methodologies
Arlington, VA
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July 20 – 24 The Quality System Regulation 21 CFR 820 and ANSI/AAMI/ISO 13485: Navigating Regulatory Requirements
Las Vegas, NV
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July 21 – 23 Design Control Requirements – Integrating the Quality System Regulation and ANSI/AAMI/ISO 13485
Las Vegas, NV
August
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August 18 – 20 Integrating Risk Management into the Product Life Cycle
Arlington, VA
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August 25 – 28 Ethylene Oxide Sterilization for Medical Devices
Arlington, VA
September
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September 1 – 3 Human Factors for Medical Devices
Arlington, VA
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September 7 – 11 AAMI/CQT Solutions Quality System
Dun Laoghaire, Dublin
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September 9 – 11 Medical Device Software Validation
Arlington, VA
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September 21 – 23 AAMI/CQT Solutions Design Control
Dun Laoghaire, Dublin
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September 21 – 25 Quality System September 2020
Arlington, VA
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September 28 – 30 AAMI/CQT Solutions Process Validation
Dun Laoghaire, Dublin
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September 30 – October 2 Design Control September 2020
Arlington, VA