SUBSTIPHARM
Emilie Verdeun is an experienced professional in the field of regulatory affairs, currently serving as the Europe Regulatory Affairs Manager and Export Regulatory Affairs Pharmacist at SUBSTIPHARM since June 2014. Prior to this position, Emilie worked at MEDIPHA SANTE from April 2011 to June 2014 as a Pharmacien Affaires Réglementaires, focusing on European procedures, national marketing authorization requests, price requests, and regulatory compliance. Emilie's early experience includes a regulatory affairs and quality assurance internship at Unither Pharmaceuticals in 2010, where responsibilities included regulatory monitoring and procedure documentation. Emilie holds a Master's degree in legal and economic strategies for marketing health products from Université Bordeaux 2 Victor Segalen, along with a pharmacy degree from the same institution.
SUBSTIPHARM
Substipharm is a privately held pharmaceutical Group. We develop, supply and commercialize pharmaceuticals in more than 60 countries worldwide. Our portfolio of products that we currently license out or distribute directly or through partners comprises more than 60 different molecules. Our development pipeline includes as well more than 40 ongoing projects. We have a successful portfolio of pharmaceutical products and vaccines including: Mature brands Generics Over the counter (OTC) pharmaceuticals Difficult to develop medicines Value added presentations Biological products including vaccines: