Camille Metais

Camille Metais is Associate Director, Regulatory Affairs in Alexion Pharmaceuticals International, Lausanne, Switzerland. Camille is responsible for the management of projects involving the design and implementation of European and global regulatory strategies for the development, registration, and maintenance of pharmaceutical and biotechnology medicinal products developed by Alexion. Her expertise is in development of regulatory strategies for drugs and biologics, especially including orphan and pediatric diseases. Before joining Alexion, Camille was Director with Voisin Consulting Life Sciences and was helping small to mid-size companies in the design and implementation of their regulatory strategies. With Voisin Consulting, Camille was heavily involved in the discussions around the implementation of the pediatric regulations. She focused on orphan products, design of Pediatric Investigation Plans and first-in-human clinical developments. Camille is an engineer by training and graduated from the Ecole Polytechnique, Paris, France where she specialized in biology and biochemistry.