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…

MDPharmaCourses | Regulatory, Quality and Compliance Training

Medical Device Sterilization Process  LIVE WEBINAR 22 February 2017 Register Now! Download the Course Brochure Duration: 50 min. + 10 min. Questions Time. Description: The course is aimed at staff of Quality Assurance, Regulatory and Research and Development of biomedical companies manufacturing of sterile medical devices, their suppliers and subcontractors. The course includes a theoretical introduction to the concept of sterilization and a description of the main sterilization methods used currently; also…

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NEW Clean Room Live Webinar: ISO 14644:2015,design and construction, compliance, personnel behaviour –  Register Now! Download the course Brochure Duration: 50 min. + 10 min. Questions Time. On Demand Fill the form below to define a suitable timeframe.    Description: Controlling contamination is essential in many manufacturing and research activities. The use of clean rooms, along with strict and stringent processes, makes this possible. ISO has a series of standards dedicated to clean…

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