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

The Why, How, When and What of the Medical Devices Regulation

With the EU Medical Devices Regulation now in force, manufacturers need to ensure they understand and are ready to meet requirements, that they have reviewed how their products will be affected by reclassification, that they have engaged with the notified bodies and that they stay up to date with developments. Listen to the PharmaLex podcast – The Why, How, When and What of the Medical Devices Regulation with our expert Jean Boudaud.

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.).