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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 GmbH, an international consulting company with subsidiaries in China and India. Under his leadership, the company group has developed into a leading provider in the field of quality and risk management. DIETZ Consultants supports leading OEMs and Tier-1s in the automotive industry worldwide as well as clients in the aerospace, defense, engineering and manufacturing technology sectors. DIETZ Consultants' FMEA forums are important events in the annual cycle for a global community of experts to exchange expertise and further develop methods.