Anne-Valérie ANGERARD
Anne-Valérie has spent more than 20 years in regulatory affairs at the headquarters of pharmaceutical companies, with product portfolio management activities (MA, variation, advertising, medical devices, etc.). She has experience of decentralized and centralized mutual recognition procedures. From 2020 to 2022, in addition to her work in the pharmaceutical industry, she became a trainer at IMIS, where she put her experience in regulatory affairs at the service of students. In 2021, she joined Blue Reg, now Cencora PharmaLex, where she is in charge of regulatory affairs consulting for pharmaceutical companies of all sizes, covering a wide range of topics: regulatory positioning and strategy, registration, life cycle management, and answering questions from the authorities.
Anne-Valérie FAUCHER
Anne-Valérie has over 20 years’ experience in regulatory affairs, including 15 years at the head office of pharmaceutical companies, with activities in EU & Rest of World product portfolio management (registration and maintenance). In Europe, she has experience of decentralized and centralized mutual recognition procedures. In 2018, she joined Blue Reg, now Cencora PharmaLex, and is in charge of regulatory affairs consulting for laboratories of various sizes on a variety of subjects: regulatory positioning and strategy, registration, life cycle management, answering questions from the authorities.