MDR Suite | General Introduction of the MDR

October 18, 2022

Date: 18 October 2022

Time: 15:00-16:30 CEST 

Location: Virtual

Language: English

Costs: € 295,-

Package deal: € 3750.-* for all 11 sessions

* Team Members with different roles and responsibilities? No problem. We offer flexible options for your company, team, or individual experts. You can send different delegates from your company to the sessions and still qualify for the package.


The Medical Devices Regulation (MDR) is the legislation setting out the requirements that manufacturers must meet in order to market medical devices in the European Union. It affects all manufacturers, importers, distributors and representatives of medical devices within the EU. The MDR, which replaces the Medical Devices Directive (93/42/EEC) and Active Implantable Medical Devices Directive (90/385/EEC). 


  • CE Mark & The EU
  • Role of Notified Bodies, Competent  Authorities and Others
  • Purpose of the MDR
  • Core changes MDD to MDR
  • Timelines
  • Q&A

Who should attend?

Manufacturers of medical devices, especially: Regulatory Affairs, Clinical Affairs Specialists and Quality Assurance specialists. 


Peter Reijntjes
Post date: February 10, 2022
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