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

IUFC

SECOND EDITION OF THE CERTIFICATE – NOVEMBER 2020 – APRIL 2021

Potential applicants are invited to attend an infosession on the 4th of November, 2020, from 17:00 to 18:00. This infosession will take place remotely, via Microsoft Teams.
Please connect via this link to attend the session.

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 2020 to April 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 :
www.medidee.com/services/caraqa-training-network


In collaboration with :