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AAMI/Kilmer Industrial Sterilization Webinar Series
June 15 to 30, 2021
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Human Factors For Medical Devices (Jun21)
June 22 to 24, 2021
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HTMLive!: Medical Device Cybersecurity: Overview of Available Resources
June 22, 2021 2:00 PM to 3:00 PM
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Integrating Risk Management into the Product Life Cycle (Jun21)
June 28 to 30, 2021
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HTMLive!: Getting the CMMS to Work for Us Phase 2: Optimizing Work Order Types
July 6, 2021 2:00 PM to 3:00 PM
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Navigating 510k and De Novo Requirements (Aug21)
August 2 to 5, 2021
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Process Validation Requirements & Industry Practices (Aug21)
August 10 to 12, 2021
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Design Control Requirements – Integrating the Quality System Regulation (Aug21)
August 17 to 19, 2021
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Ethylene Oxide Sterilization for Medical Devices (Aug21)
August 30 to September 2, 2021
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Human Factors for Medical Devices (Sept21)
September 8 to 10, 2021
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EUROPE: Integrating Risk Management into the Product Life Cycle (Sep21)
September 13 to 15, 2021
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Quality System Regulation 21 CFR 820 and ANSI/AAMI/ISO 13485 (Sept21)
September 20 to 24, 2021
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Industrial Sterilization for Medical Devices (Sept21)
September 27 to 30, 2021
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Integrating Risk Management into the Product Life Cycle (Oct21)
October 4 to 6, 2021
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Radiation Sterilization for Medical Devices (Oct21)
October 25 to 28, 2021
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Design Control Requirements – Integrating the Quality System Regulation (Nov21)
November 8 to 10, 2021
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Quality System Regulation 21 CFR 820 and ANSI/AAMI/ISO 13485 (Nov21)
November 15 to 19, 2021
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COSTA RICA: Process Validation Requirements & Industry Practices (Dec21)
December 7 to 9, 2021
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