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EU regulation on medical devices (MDR) and on in vitro diagnostic devices (IVDR)

26.9.2024 08:30

webinar

Schedule:

Thursday 26th of September at 8.30-12.00 and 
Friday 27th of September at 8.30-12.00.

Content of the Online Training

Day 1:
Scope and definitions

  • Scope of the MDR 2017/745 and products that fall within the definition of a medical device
  • Scope of the IVDR 2017/746 and products that fall within the definition of an in vitro diagnostic medical device

Economic Operators

  • Who are they? What are their roles and responsibilities?
    • A European authorized representative
    • A distributor
    • An importer
    • A manufacturer
    • A person responsible for regulatory compliance

Classification of medical devices under MDR and in vitro diagnostic medical devices under IVDR

  • Intended purpose
  • Qualification of medical device / in vitro diagnostic medical device
  • Risk based classification
  • Rules of medical device/ in vitro diagnostic medical device classification

Conformity assessment routes and the role of Notified Bodies

  • Quality management system requirements and ISO 13485
  • What is a Notified Body?
  • Explanation of different conformity assessment routes
  • CE marking

Day 2:

Key elements of technical documentation

  • Device description and specification
  • Information to be supplied by the manufacturer
  • Design and manufacturing information
  • General safety and performance requirements
  • Benefit-risk analysis and risk management
  • Product verification and validation
  • Post-market surveillance

Clinical evidence

  • MDR 2017/745: Clinical Evaluations
    • Clinical performance
    • Clinical investigations
    • Post-market clinical follow-up
  • IVDR 2017/746: Performance evaluations
    • Scientific validity
    • Analytical performance
    • Clinical performance
    • Performance studies
    • Post-market performance follow-up

Post-market surveillance and vigilance

  • Requirements after product launch e.g., information gathered by manufacturer in cooperation with other economic operators
  • Reporting requirements of serious incidents and field safety corrective actions

 

Interactive elements can be included using e.g. Socrative, Kahoot or Mentimeter. Training will be held in English in Teams.

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Event time

Starts:   26.9.2024 08:30
Ends:   27.9.2024 12:00

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Event location

webinar


Organizer

Loimu ry

09-6226850

urapalvelut@loimu.fi

www.loimu.fi