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Daniëlle Sleegers

Director Regulatory Affairs & PRRC
MedEnvoy Global

Daniëlle has more than 14 years of experience in the medical device industry and has been hands-on in international registrations, post-market surveillance, clinical evaluations, and risk management. She has a master’s degree in Biopharmaceutical Sciences and has worked at the Medicines Evaluation Board of the Netherlands for 5 years before her transfer to the medical device industry.

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