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    Implementation of the Medical Device Regulation 2017/745 (MDR) for CE Marking

    Implementation of the Medical Device Regulation 2017/745 (MDR) for CE Marking

    Level Implementation Duration 3 days
    Available to book: Virtual classroom See all dates and book
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    This three-day course from your partner in learning is especially useful for regulatory affairs, quality management and quality assurance professionals who need to implement the medical device regulation (MDR). The MDR training is also designed for people working for organizations that partner with Medical Device manufacturers.

    You will learn all the requirements needed for conformity assessment, how to fulfil technical documents and how to plan post-market activities required by the MDR. By the end of the course you will be able to put all this knowledge into working practice in your organization.

    With the opportunity to gain eight CPD points on completion and comprehensive training notes, this MDR training is everything you need to guide and support others.

    How will I benefit?

    This course will help you:

    • Comprehensive understanding of the European medical devices regulation
    • Support other people and partner organizations affected by MDR
    • Organize required documentation
    • Follow the necessary steps for your organization to meet the MDR requirement MDR 4

     

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    This training course is HRD Corp claimable programme.

    • By the end of the course delegates will be able to:

      • Develop a strategy for regulatory compliance as stipulated by MDR
      • Implement requirements concerning the following steps for Conformity Assessment:
        • Scope and applicability of MDR
        • EU risk classification criteria for medical devices to determine “Risk Class”
        • General Safety and Performance Requirements (GSPRs) as the basis for CE marking, including the use of standards
        • Conformity assessment routes and their application based on risk class
        • Self-certification, CE-certification by Notified bodies, involvement of authorities, scrutiny
        • ‘Declaration of Conformity’ and CE marking
      • Fulfil Technical Documentation requirements, e.g. in
        • Putting together ‘Technical Documentation’
        • Necessary control of outsourced activities and processes and roles of external partners (e.g. supplying and commercial)
        • Instantiate the importance and role of clinical data
        • Risk management, process validation and their regulatory significance
        • Drawing up Instruction For Use, label and other information supplied with the device
        • Consistency and validity of information and electronic data management
      • Plan post-market activities required by MDR with respect to:
        • Risk Management and related planning
        • Post-Market Surveillance and Post-Market Follow-Up (PMCF)
        • Periodic reports, Vigilance, ad-hoc reporting
        • Regulatory responsibilities of all economic operators including communication with competent authorities, notified bodies, economic operators, customers etc.
        • Recall, Field Safety Corrective Actions (FSCA), Corrective And Preventative Action (CAPA)
        • Regulatory relevance of change control to QMS, design and manufacturing
        • Extent of readiness for audits/reviews/assessment
      • Put into effect gained knowledge concerning implementation of MDR requirements into your organization, e.g. in projects for CE-marking

    • The course is especially suitable for:

      • RA, QM, and QA professionals who need to implement the MDR
      • Anyone concerned with certification or active in projects for CE-marking
      • Staff working for organizations that partner with Medical Device manufacturers e.g. as subcontractor, crucial supplier, OEM, Authorized representative, importer, distributor, auditee

    • You must have a good understanding of the requirements in the MDR, which is conveyed by our one-day Requirements training course or our MDD to MDR transition course.

      You should also have either experience with, or basic knowledge, of quality management systems for the medical device industry, or good understanding of European Medical Device legislation, or some experience in pre-or post-market activities within the EU.

      Please note:
      This course will not cover implementation for In Vitro Diagnostics or concentrate on devices with specific requirements.

       

    • To qualify for the HRD Corp Claimable Course, your company must be registered with HRD Corp and comply with the grant requirements. We suggest consulting with your Human Resources team to confirm your eligibility and understand the application process. Once we receive your booking, our team will provide you with the necessary documents and further details to support your HRD Corp grant application.

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

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