Live Webinar – Regulation 745/2017 on Medical Devices: Technical File structure BUY NOW DURATION: 50 min + 10 min. Question Time Description: Prerequisite: Basic knowledge of medical devices Recipients: Quality Assurance, Regulatory, Top Management of companies that manufacture, Import Distribute medical devices in Europe and their suppliers Contents: Annex I and Annex II of MDR; main contents expected in the technical file. Why You Should Attend: The new Regulations on medical devices…

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