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Human Factors for Medical Devices (Nov21)
November 30 to December 3, 2021Register
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Navigating 510k and De Novo Requirements (Dec21)
December 6 to 9, 2021Register
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HTMLive!: Defendable Measurements: Importance of Accuracy...(Dec21)
December 14, 2021Register
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Using Risk Management Standard EN ISO 14971:2019 Under the MDR and IVDR
December 15, 2021Register
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Industrial Sterilization for Medical Devices (Jan22)
January 18 to 21, 2022Register
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HTMLive!: Artificial Intelligence in Healthcare Roundtable
January 25, 2022Register
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Medical Device Cybersecurity 101 for HTM Professionals (Jan2022)
January 25 to 27, 2022Register
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Quality System Regulation 21 CFR 820 and ANSI/AAMI/ISO 13485 (Jan22)
January 31 to February 4, 2022Register
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Integrating Risk Management into the Product Life Cycle (Feb22)
February 9 to 11, 2022Register
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Design Control Requirements – Integrating the Quality System Regulation (Feb22)
February 23 to 25, 2022Register
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Navigating 510k and De Novo Requirements (Mar22)
March 1 to 4, 2022Register
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Human Factors for Medical Devices (Mar22)
March 8 to 10, 2022Register
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Ethylene Oxide Sterilization for Medical Devices (Mar22)
March 22 to 25, 2022Register
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Production & Quality System Software (April22)
April 4 to 5, 2022Register
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Process Validation Requirements & Industry Practices (April22)
April 6 to 8, 2022Register
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Medical Device Software Validation (April22)
April 11 to 13, 2022Register
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Quality System Regulation 21 CFR 820 and ANSI/AAMI/ISO 13485 (April22)
April 18 to 22, 2022Register
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Integrating Risk Management into the Product Life Cycle (May22)
May 4 to 6, 2022Register
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Industrial Sterilization for Medical Devices (May22)
May 10 to 13, 2022Register
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Design Control Requirements – Integrating the Quality System Regulation (May22)
May 23 to 25, 2022Register
