Refine Results
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Industrial Sterilization for Medical Devices (Jan 2021)
January 19 to 22, 2021Register
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Design Control Requirements – Integrating the Quality System Regulation (Feb21)
February 8 to 10, 2021Register
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Integrating Risk Management into the Product Life Cycle (Feb21)
February 17 to 19, 2021Register
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Sampling Plans Made Easy
February 25 to March 1, 2021Register
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Quality System Regulation 21 CFR 820 and ANSI/AAMI/ISO 13485 (Mar21)
March 1 to 5, 2021Register
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Human Factors for Medical Devices (Mar21)
March 8 to 10, 2021Register
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Ethylene Oxide Sterilization for Medical Devices (Mar21)
March 15 to 18, 2021Register
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COSTA RICA: Quality System Regulation 21 CFR 820 and ANSI/AAMI/ISO 13485 (Mar21)
March 22 to 26, 2021Register
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Production & Quality System Software (Mar21)
March 29 to 31, 2021Register
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Medical Device Software Validation (Mar21)
March 31 to April 2, 2021Register
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EUROPE: Design Control Requirements - Integrating the QSR (Apr21)
April 12 to 14, 2021Register
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Process Validation Requirements & Industry Practices (Apr21)
April 14 to 16, 2021Register
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Navigating 510k and De Novo Requirements (Apr21)
April 26 to 29, 2021Register
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Industrial Sterilization for Medical Devices (May21)
May 4 to 7, 2021Register
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Quality System Regulation 21 CFR 820 and ANSI/AAMI/ISO 13485 (May21)
May 10 to 14, 2021Register
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Design Control Requirements – Integrating the Quality System Regulation (May21)
May 25 to 27, 2021Register
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Purchasing Controls & Supply Chain Management (Jun21)
June 14 to 16, 2021Register
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Corrective & Preventive Action Requirements & Industry Practice (Jun21)
June 17 to 18, 2021Register
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Human Factors For Medical Devices (Jun21)
June 22 to 24, 2021Register
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Integrating Risk Management into the Product Life Cycle (Jun21)
June 28 to 30, 2021Register