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20 Jul

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

24 Aug

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

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2017/745 capa clean room clinical evaluation Complaint form compliance training contamination control corrective action corso in italiano course DESIGN CONTROL design input design output design validation design verification emdr FDA form iso 10993 ISO 13485 live webinar meddev meddev 2.7.1 medical device medical device training new mdr new medical device regulation pharmaceutical manufacturing preventive action quality 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 warning letter webinar

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

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