Martine Dehlinger-kremer PhD

Dr. Dehlinger-Kremer has more than 30 years of experience in the research industry, including more than 26 years of progressively higher levels of Regulatory and Medical Affairs leadership responsibility. For 21 years, she served as a Vice President of International and Global Regulatory and Medical Affairs at various CROs headquartered in the U.S. Martine has contributed to the global development of numerous products, including orphan drugs and biosimilars. She has participated in 100+ NDAs/MAAs in local and CTD/eCTD/NeeS format, in the maintenance of products on the market, and in numerous clinical studies across all phases. She has also served as the chair of the Pediatric Working Group of EUCROF, and as lead member of the Pediatric Franchise at Research Pharmaceutical Services, a division of PRA International. Dr. Dehlinger-Kremer holds a PhD from the University of J.W. Goethe in Frankfurt, Germany; a general academic studies degree in neurophysiology from the Louis Pasteur University in Strasbourg, France; and a Master of Sciences degree from the University Moulin de la Housse in Reims, France. She is also a registered member of The Organization for Professionals in Regulatory Affairs (TOPRA).