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    • Directive 93/42/EEC – MDD – Medical Devices Directive with 2007/47/EC – Consolidated Version
    • GHTF – Global Harmonization Task Force – Guidelines
    • MDD 93/42/EEC of 14 June 1993 concerning medical devices – Original directive
    • TITLE 21CFR 820 QUALITY SYSTEM REGULATION
    • Directive 90/385/EEC – AIMDD – Active Implantable Medical Devices Directive – Consolidated Version
    • DIRECTIVE 98/79/EC – IVD – In vitro diagnostic medical devices – Consolidated Version
    • Canada Medical Devices Regulation
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capa clean room clinical evaluation contamination control corso in italiano course DESIGN CONTROL design input design output design validation design verification dispositivi medici emdr FDA FDA REGULATION ISO 13485 iso 13485 training iso 13485:2016 IVD live webinar mdd meddev meddev 2.7.1 medical device Medical Device Manufacturing medical devices New ISO Medical Device new mdr new medical device regulation pharmaceutical manufacturing QMS quality quality system management quality training regulatory regulatory affairs regulatory course tech file technical file training udi Unique Device Identification VALIDATION validazione webinar

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