Live Webinar: Drafting of the Biocompatibility report in accordance with ISO 10993-1
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The course is aimed at staff of Quality Assurance, Regulatory, and research and development of biomedical companies legalii manufacturers of medical devices of any class, who are in contact with the human body. The course describes the ‘risk-based approach in the planning of biocompatibility tests in vitro and in vivo. Level: Intermediate, it requires basic knowledge of Directive DM.