Implementation of the Medical device regulation 2017/745 (MDR) for CE Marking Classroom Training

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?

  • 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