Join
Events
2019
April
May
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May 6 AAMI/RD - Renal Disease and Detoxification Committee Meeting
Arlington, VA
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May 7 – 9 Software Validation Workshop: Practical Tools and Techniques
Arlington, VA
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May 7 – 9 Regulatory Requirements for Software Validation - May 2019
Arlington, VA
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May 14 – 17 Industrial Sterilization for Medical Devices - May 2019
Arlington, VA
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May 19 – 25 Healthcare Technology Management Week
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May 20 – 21 AAMI/BSI Workshop on AI and Machine Learning Algorithms
Arlington, VA
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May 21 WEBINAR: HTM Best Practices in Large Health Systems
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May 23 Webinar: Using HTM Data to Drive High Reliability Healthcare
June
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June 7 AEM Workshop - Cleveland, OH
Cleveland, OH
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June 7 HTM Annual Leadership Exchange (HALE)
Cleveland, OH
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June 7 – 10 AAMI Exchange 2019
Cleveland, OH
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June 10 – 11 AAMI SM-WG05 Device Security Working Group
Arlington, VA
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June 11 – 13 AAMI/ID, Infusion Devices Committee
Arlington, VA
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June 12 – 14 AAMI/SM/WG 03, Interoperability Working Group Meeting
Arlington, VA
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June 18 – 19 Corrective and Preventive Action Requirements and Industry Practice-June 2019
Arlington, VA
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June 19 – 21 Purchasing Controls & Supply Chain Management - June 2019
Arlington, VA
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June 24 – 28 The Quality System Regulation 21 CFR 820 and ANSI/AAMI/ISO 13485: Navigating Regulatory Requirements-June 2019
Arlington, VA
July
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July 8 ST/WG 84 Endoscope Reprocessing Meeting
Arlington, VA
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July 9 – 11 AAMI CN/WG 01, Luer activated valves Meeting
Arlington, VA
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July 15 – 16 Joint Meetings of the AAMI Health IT Committee
Arlington, VA
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July 15 – 16 Joint Meetings of the AAMI Health IT Committee
Arlington
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July 16 WEBINAR: Mnthly Wrkld Tracker by Technician Using Data Modl
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July 30 – August 1 Integrating Risk Management into the Product Life Cycle - July 2019
Arlington, VA
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 – 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 Course
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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
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 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 13 – 15 Risk Management - November 2019
Arlington, VA
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November 19 – 21 Human Factors for Medical Devices - November 2019
Arlington, VA