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    Medical Device CE Marking Requirement

    Medical Device CE Marking Requirement

    Duration 3 days
    Available to book: Public classroom PHP2800 View dates and book now
    Available to quote: In-house Get quotation for in-house training
    Available as an In-House Course

    Call us and speak with our training advisors on running an in-house training.

    • Suitable for large groups
    • Flexible & convenient
    • Tailored for your needs
    Learn more about in-house training

    This course will teach you how to start making informed decisions with regards to meeting the requirements of the EU Medical Devices Directives. On completion of the training, participants will be able to identify the steps required to reduce the risks and uncertainty in the EU regulatory process and thus save time bringing products to the EU market.

      • Explain the European CE marking approach with respect to medical devices, active 
        implantables and IVDs, including borderlines with other products, as covered by the three 
        Council Directives (MDD, AIMDD, IVDD) and the underlying Commission Directives such as the animal tissue directive and blood derivative directives
      • Prepare a clinical evaluation in accordance with MED DEV 2.7.1 and GHTF Guidance 
        Documents
      • Explain the significance of the EU risk classification criteria for medical devices in 
        determining the conformity assessment routes and quality assurance requirements for the 
        various risk classes, as well as the routes to compliance for borderline products that include pharmaceuticals, human derivatives and/or engineered tissues
      • Describe the role of the essential requirements as the basis for CE marking, including the 
        use of standards
      • Describe the role of clinical data and risk management
      • Identify the necessary steps required for post market surveillance and for reporting adverse incidents under the vigilance system
      • Identify technical documentation requirements.
      • Senior management
      • Regulatory, quality, design, development, manufacturing, marketing managers and 
        personnel
      • Organizations preparing "own branding" or "private labelling" of devices
    • This training course is HRDF approved under the SBL scheme.

      On completion, you will be awarded an internationally recognized BSI Training Academy certificate.

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