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31 Oct

Training New MDR Regulation 2017/745 on Medical Devices: technical file structure

24 Jan

Live Webinar: Drafting of the Biocompatibility report in accordance with ISO 10993-1

13 Dec

Live Webinar Validation of industrial processes (IQ/OQ/PQ) and technology transfer in accordance with ISO 13485: 2016

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MDPharmaCourses | Regulatory, Quality and Compliance Training
Regulation 745/2017 on Medical Devices: technical file structure – Live Webinar
MDPharmaCourses | Regulatory, Quality and Compliance Training
Regulation 745/2017 on Medical Devices: Unique Device Identification
MDPharmaCourses | Regulatory, Quality and Compliance Training
Live Webinar: Regulation 745/2017 on Medical Devices: post market activities and follow up
MDPharmaCourses | Regulatory, Quality and Compliance Training
Regulation 745/2017 on Medical Devices: main changes and timeline to implementation

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