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 Report of the clinical data to be included in the dossier of the product Technical according…

MDPharmaCourses | Regulatory, Quality and Compliance Training

Live Webinar – Technical File Structure according to New Medical Device Regulation Register Now! Duration: 50 min. + 10 min. Questions Time. 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 structure and content of a technical file and its main attachments for the CE marking of a medical device. LEVEL: INTERMEDIATE…

MDPharmaCourses | Regulatory, Quality and Compliance Training

NEW EU Medical Device Regulations 2016-Live Webinar  Register Now! Download the course Brochure  Duration: 50 min. + 10 min. Questions Time. ON DEMAND: Fill the form below to schedule the live webinar on demand session: Description: This live webinar course will provide guidance on the new requirement introduced with NEW EU Medical Device Regulation. In Particular will discuss the following points: Main New Requirements (UDI) Unique Identification number Post market activities New Technical…

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