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    Requirements of the Medical Device Regulation (MDR) Training Course

    Requirements of the Medical Device Regulation (MDR) Training Course

    Level Understanding Duration 1 day
    Available to book: Public classroom HK$3360 Book your place

    This course is now available online

     

    The course will give you an understanding of the key requirements, which will provide: 

    • Essential knowledge to understand Regulatory Affairs of medical devices in EU, e.g. in the position of top management, or a manager or project member in QM/QA, R&D, design, manufacturing, supply chain, customer service and sales
    • The ability to understand the demands of the subcontractor, supplier, OEM, authorized representative, importer, distributor, allowing better relationships between them and the legal manufacturer

    How will I benefit?

    This course will help you:

    • Understand the key requirements and concepts of the European Medical Devices Regulation
    • Communicate the impact of the key requirements introduced by the MDR to your organization

     

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

      • Communicate the key requirements and concepts within the Regulation
      • Reference the necessary aspects to evaluate if and how your company is affected by MDR and to what extent
      • Define the vocabulary used within MDR
      • Explain the structure and administration of the Regulation
      • Recognize partners of manufacturers affected by the Regulation
      • Describe key steps of a conformity assessment
      • Explain the main impacts on the QMS relating to MDR
      • Recognize requirements for post-market surveillance and updates 
      • New starters in Regulatory Affairs (RA), personnel increasing their responsibility in this area, and RA professionals who are not familiar with the European MDR
      • Personnel working with Regulatory Affairs departments, e.g. top management, manager or project member in QM/QA, R&D, design, manufacturing, supply chain, customer service and sales
      • Staff working for organizations that partner with Medical Device manufacturers, e.g. as subcontractor, supplier, OEM, authorized representative, importer, distributor, auditee etc. 
      • You will gain 8 CPD points on completing the course
      • Training course notes
      • Lunch
      • Refreshments 
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