Morgane has been supporting and advising manufacturers of health products and similar products (including drugs, medical devices, medical devices, cosmetics, supplements and foodstuffs) for about fifteen years on all legal and regulatory issues that they may encounter throughout the life cycle of products or companies (early access, market access, intervention of notified bodies, communication, anti-corruption measures, etc.) in order to help them comply with regulations. His intervention for service companies mainly concerns innovative projects or innovative structures to be validated or determined, in particular in digital health, telemedicine or tele-expertise and more generally electronic health.

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She also assists companies during their interactions with public authorities (project or decision/decision/inspection/audit by the ANSM and the DGCCRF) in the pre-litigation phase, through the implementation of corporate policies or training courses. Her assistance covers litigation matters, and she deals with cases involving liability for defective products and commercial law.

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In addition to this expertise in consulting and litigation, Morgane also offers contract assistance to its clients marketing health and similar products, service companies, as well as CDMOs and manufacturers, mainly concerning contracts governing development or marketing in B2B or contracts with health professionals. As part of corporate transactions in the field of Life Sciences, it provides regulatory assistance.

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Morgane has also been involved in the implementation of clinical trials as a member of a Personal Protection Committee since 2021. She also participates as Pro Bono to projects carried out by various agencies and/or the Ministry of Health.

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Morgane started her career in English law firms (Simmons & Simmons, Dechert) and then joined French firms (Fidal, LPA Law) in order to structure and develop their health activities.