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Medical Device Trainings

Regulatory, Quality and Compliance Webinar

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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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  • A stethoscope in front of medical

    Clinical Evaluation of Medical Device – Commented Interactive Presentation Webinar

    €125.00
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  • clinicalEV

    Live Webinar Clinical Evaluation and literature data according to MEDDEV 2.7.1 rev June 2016 – May 29

    €275.00
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  • NEW EU REGULATION_2

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

    €275.00
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  • NEW EU REGULATION_2

    Regulation 745/2017 on Medical Devices: obligations of the economic operators, from Eudamed registration to Responsible person

    €275.00
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  • NEW EU REGULATION_2

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

    €275.00
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  • NEW EU REGULATION_2

    Regulation 745/2017 on Medical Devices: technical file structure

    €340.00
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  • NEW EU REGULATION_2

    Regulation 745/2017 on Medical Devices: Unique Device Identification

    €275.00
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