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FMEA for Medical Devices. Risk analyses for product design and manufacturing processes.
The analysis of technical risks is legally regulated for medical devices. In addition, there are industry-specific, national, and international standards. DC ONLINE presents tailored approaches in the context of FMEA applications.
ImportantThis event does not currently have an available date. Please contact us if you are interested.
Scope of services

  • Tailored information at the highest quality level
  • Each participant receives a training certificate
  • Each participant receives the webinar training material

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    Benefit

    Implementing the required risk assessments in the context of product approval.
    Group of participants

    The DC Online event is aimed at professionals and executives responsible for conducting technical risk analysis of medical devices.
    Participant fee
    The participation fee is 138,00€ (net)