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Medical Device Trainings

Regulatory, Quality and Compliance Webinar

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  • Upcoming Live 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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  • Complaint_handling-1-1024x768 (1)

    Complaint Handling in Compliance with FDA and ISO Regulations

    €285.00
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  • Complaint_handling-1-1024x768 (1)

    Complaint Handling in Compliance with FDA and ISO Regulations

    €385.00
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  • audit_complaint_practice

    How FDA Trains Its Investigators to Review CAPA, and Best Practices for Preparation

    €285.00
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  • audit_complaint_practice

    How FDA Trains Its Investigators to Review CAPA, and Best Practices for Preparation

    €285.00
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  • audit_complaint_practice

    How FDA Trains Its Investigators to Review CAPA, and Best Practices for Preparation – 19 June

    €285.00
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  • Sale! Tech_file

    Live Webinar – Technical File Structure according to New Medical Device Regulation – Recorded

    €265.00 €235.00
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  • Tech_file

    Live Webinar – Technical File Structure according to New Medical Device Regulation -ON DEMAND

    €325.00
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  • UDI_BAR_CODE

    Live Webinar (UDI) Unique Device Identification according to New Medical Devices Regulation – 05 May

    €275.00
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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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  • Sale! medical-devices

    Medical Devices and applicable Regulations – Commented Interactive Presentation Webinar

    €195.00 €135.00
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