A Louvain-la-Neuve
17 crédits
Horaire adapté - En anglais
Sigle du programme : MEDE2FC
Mémoire/Travail de fin d'études : OUI
Stage : NON
Activités en anglais : OUI
Activités en d'autres langues : NON
Activités sur d'autres sites : NON


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Potential applicants are invited to attend an infosession on the 9th of June, 2021. The infosession could be attended :

Please contact caraqa@uclouvain.be if you want more information

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

This continuing education programme will consist of four modules organized from November 2021 to April 2022. 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 Belgium, Switzerland, Germany and Denmark. For more information, go to :

Votre profil

  • 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 :