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Manon Gielkens

Principal Regulatory Affairs Specialist
Medtronic, Afghanistan

Manon Gielkens has over 8 years experience in the clinical regulatory field in the EMEA region. In addition to her experience with the submission process of Clinical Investigation Applications in this region, she is also involved in the implementation of the EU MDR in her company. Among her responsibilities, is the EUDAMED Clinical Module where she leads activities on the playground review which includes providing feedback to the Commission in collaboration with MedTech.

Disclosure information not submitted.

Presentation(s):