Connie van Oers
Dr. Connie van Oers has been educated in Molecular Sciences followed by a PhD in Molecular Biology. She has over 20 years experience in Life Science industry of which about 15 years in Regulatory Affairs. She has a broad experience in management of regulatory submissions of both marketed and innovative medicinal products. She was manager Regulatory Affairs, Quality Assurance and Pharmacovigilance for the Dutch affiliate of a multinational pharmaceutical company. Currently, she is managing consultant of an experienced team of consultant dealing with various aspects of regulatory affairs, including Program Management and ATMPs.