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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 contact caraqa@uclouvain.be if you want more information
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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
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New European regulation requiring experts in the field
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Critical know-how to boost innovation management in MedDev and IVD companies
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Crucial demand of start-ups, medium and large companies for this expertise
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Limited training offer in Benelux
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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 :
