17 crédits
Horaire adapté - En anglais
Stage : NON
Activités en d'autres langues : NON
Introduction
THIRD EDITION OF THE CERTIFICATE, UPCOMING – JANUARY 2022 – MAY 2022 (approximate schedule) The last infosession took place on the 4th of November. Slides are available here. |
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 academia from Belgium, Switzerland, Germany and Denmark. For more information, go to https://caraqa.com
Votre profil
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Biomedical, mechanical, electronic, software or material science engineers, in charge of medical or IVD development projects
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Physicians, scientists or inventors of biomedical devices
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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
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Specialists involved in the design of sensitive medical products
In collaboration with :
