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WHO Global Model Regulatory Framework for Medical Devices Including in Vitro Diagnostic Medical Devices

Also, it describes circumstances in which a regulatory authority may either "rely on" or "recognize" the work products from trusted regulatory sources (such as scientific assessments, audit, and inspection reports) or from the WHO ...

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WHO Global Model Regulatory Framework for Medical Devices Including in Vitro Diagnostic Medical Devices

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Length: 72 pages

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