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emdr

22
Dec

Live Webinar Clinical Evaluation and literature data according to MEDDEV 2.7.1 rev June 2016

Live Webinar Clinical Evaluation and literature data according to MEDDEV 2.7.1 rev June 2016   DURATION: 50 min + 10 min. Question Time BUY 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…

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MDPharmaCourses | Regulatory, Quality and Compliance Training
22
Dec

Regulation 745/2017 on Medical Devices: main changes and timeline to implementation

Live Webinar – Regulation 745/2017 on Medical Devices: main changes and timeline to implementation  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: The Commission position on medical devices; regulation implementation timeline, main impacts on existing devices, main impacts on new devices, strategies…

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MDPharmaCourses | Regulatory, Quality and Compliance Training
22
Dec

Live Webinar: Regulation 745/2017 on Medical Devices: post market activities and follow up

Live Webinar – Regulation 745/2017 on Medical Devices: post market activities and follow up 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: Required updates of Technical File over time; methods for post market follow up according to a risk-based approach. Why You Should…

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MDPharmaCourses | Regulatory, Quality and Compliance Training
22
Dec

Regulation 745/2017 on Medical Devices: Unique Device Identification

Live Webinar – Regulation 745/2017 on Medical Devices: Unique Device Identification 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: Unique identification number composition; where and how it is placed; UDI as part of the traceability Why You Should Attend: On 5 April, 2…

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