Jeanne Fabre is an associate in the Paris office of Latham & Watkins and a member of the firm's Healthcare & Life Sciences Practice. She advises multinational companies and start-ups in the pharmaceutical, biotech, medical devices, cosmetics, and food and beverage sectors on a broad variety of complex European, domestic and cross-border regulatory matters, including clinical trials, product approvals, market access, promotion and advertising, post-market obligations, contracts, and general compliance matters.
Ms. Fabre has experience working in pharmaceutical companies. Since her Master II, she has worked more than three years for several companies both for local affiliates and parent company. She was part-time seconded for 18 months to a pharmaceutical company specialized in rare diseases, and a further three months for another pharmaceutical company. She worked on a wide range of regulatory topics (such as observational, ATU and post-ATU studies, service providers, consultancy and pay for performance agreements, pricing topics).
Ms. Fabre's experience includes advising:
*Matter handled prior to joining Latham