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Latest Events

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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2017/745 biocompatibility biocompatibility webinar biological evaluation biological safety capa clinical evaluation Complaint form corrective action course DESIGN CONTROL design input design output design validation design verification emdr FDA fda training form iso 10993 ISO 13485 live webinar meddev meddev 2.7.1 medical device medical device training new mdr new medical device regulation preventive action quality system management regulatory regulatory affairs regulatory course tech file technical file template training udi udi training udi webinar Unique Device Identification unique device identification webinar VALIDATION warning letter webinar

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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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