At Louvain-la-Neuve
17 credits
Customized schedule - In English
Programme acronym: MEDE2FC
Dissertation/Graduation Project : YES
Internship : NO
Activities in English: YES
Activities in other languages : NO
Activities on other sites : NO


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Online infosessions will take place on Thursday, September 29th at 17:00 (registration form) and Monday, November 7th at 17:00 (registration form).

Please contact if you want more information.

The Louvain School of Engineering of UCLouvain and Medidee jointly organise a new University Certificate in “ : Clinical, regulatory and quality affairs for medical devices and in-vitro diagnosis”.

This continuing education programme will consist of four modules organized from January 2023 to June 2023. Classes will be held in Louvain-la-Neuve and will consist of more than 170 hours of training.

Highlights of the programme
  • New European regulation requiring experts in the field

  • Critical know-how to boost innovation management in MedDev and IVD companies

  • Crucial demand of start-ups, medium and large companies for this expertise

  • Limited training offer in Benelux

  • Covers the requirements of MDR / IVDR Article 15 “ Person responsible for regulatory compliance

This programme has been designed in accordance with the “CARAQA” international training network, including academia from Belgium, Switzerland, Germany and Denmark. For more information, go to

Your profile

  • Biomedical, mechanical, electronic, software or material science engineers, in charge of medical or IVD development projects

  • Physicians, scientists or inventors of biomedical devices

  • Employees within the regulatory, clinical and/ or quality department of a manufacturing or subcontracting company manufacturing medical devices or IVD, or in a healthcare organization

  • Specialists involved in the design of sensitive medical products

In collaboration with :