Omar Lalhou

Biography

Expert in Quality regulations, staMD from the Medical University of Warsaw, board-certified in Internal Medicine. Marcin is a drug development and medical affairs expert with over 20 years of senior medical roles in large and small pharma companies. At Bristol-Myers Squibb he was medical director for the development of garenoxacin and the European medical lead for HIV. He later worked at Chiron Biopharmaceuticals as Senior Director for Infectious Diseases and General Medicine, where he was responsible for the European registration of daptomycin. In 2008 MPh. D., Univ. Monastir, Tunisia; M. B. A., Ecole Nationale des Ponts et Chaussées, Paris, France. Omar has 15 years of experience in regulatory affairs, starting as Regulatory Affairs and Safety Manager in Pfizer’s Francophone African Region. Later he became Manager of Pfizer’s Global Manufacturing and Quality Operations at their headquarters in New Jersey; Director, Regulatory Affairs at Lumavita AG, where he was instrumental in the establishment and implementation of regulatory development plans from preclinical up to Phase I and Phase IIb approvals in the EUarc

Research Interest

regulatory affairs, starting as Regulatory Affairs and Safety