The course is aimed at Quality Assurance personnel, Regulatory and Research and Development of biomedical companies, medical device manufacturers of any class, agents and distributors. The course describes the main methods for writing an Evaluation Report of the Clinical Evaluation to be included in the product Technical dossier according to the new MEDDEV 2.7.1 guideline Rev June 2016. […]

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Live Webinar Clinical Evaluation and literature data according to MEDDEV 2.7.1 rev June 2016 – May 29 Register Now! Description: The course is aimed at Quality Assurance personnel, Regulatory and Research and Development of biomedical companies, medical device manufacturers of any class, agents and distributors. The course describes the main methods for writing an Evaluation […]

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