Clinical, regulatory and quality affairs for medical devices and in-vitro diagnostic (CARAQA)



Potential applicants are invited to attend an infosession on the 26th of August, 2020, from 17:00 to 18:00. This will take place in Louvain-la-Neuve, building “Maxwell” (Place du Levant), floor +1 – room “Shannon”. The nearest parking is “Parking Rédimé”, reachable via Avenue Georges Lemaître.

This infosession could also be attended remotely, via Microsoft Teams.
Please connect via this link to attend the session.

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 September 2020 to February 2021. 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 :

In collaboration with :