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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.
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)
    Speaker of the presentationsHere you can see the speaker who will give the presentations at the event.
    Dipl.-Ing. Winfried Dietz

    Dietz Consultants GmbH
    www.dietz-consultants.com

    Winfried Dietz is the founder and managing partner of DIETZ Consultants with subsidiaries in Asia and North America. He shoulders the responsibility of the FMEA business area development. Winfried Dietz has more than 30 years of practical experience, 25 years thereof as a consultant, trainer and coach. Other areas of interest and work include APQP, 8D, PPAP and functional safety and their interactions. Winfried Dietz is the organiser of the annual Osnabrück FMEA Forum.