PharmaLex Talks

4: The Why, How, When and What of EU MDR Regulation


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Jean has extended experience in all phases of the product lifecycle, driving compliance from concept initiation through to commercialisation and post-market support.  He provides Regulatory and Quality Assurance expertise to a broad range of companies from start-ups to multinationals and supports projects involving various medical technologies. He is bilingual in French and English and holds a Masters’ Degree of Engineering (MEng.). 
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