CARAQA.be: Clinical, regulatory and quality affairs for medical devices and in-vitro diagnosis

IUFC

Potential applicants are invited to attend an infosession
on the 6th of September, 2019, from 14:30 to 16:30.

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 (https://cutt.ly/OoSUuO).

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 October 2019 to April 2020. Classes will be held in Louvain-la-Neuve and will consist of more than 180 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 :


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