Moheb Nasr

Dr Nasr serves as a senior regulatory advisor for several biopharmaceutical companies in US, Europe, and Asia. In addition, Dr Nasr continues to play a leading role in global regulatory harmonization and introduction of modern pharmaceutical manufacturing platforms, including Continuous Manufacturing. Dr. Nasr retired from GSK in August 2017. AT GSK, Dr Nasr was responsible for the development and the execution of GSK global CMC regulatory strategy. In recognition of his scientific contributions and visionary leadership, Dr Nasr is an elected GSK Senior Research Fellow. Prior to joining GSK, Dr. Nasr spent over 22 years at US FDA. At FDA, Dr. Nasr was the head of FDA/CDER CMC regulatory office. Dr. Nasr represented FDA and PhRMA at ICH and was instrumental in the development of the Quality by Design (QbD) concept and several regulatory ICH guidelines. Dr. Nasr obtained his Pharmacy degree at the University of Cairo, Egypt, and his Ph.D. degree in Chemistry at the University of Minnesota in Minneapolis, Minnesota, USA. Dr. Nasr is an elected Fellow of the American Association of Pharmaceutical Scientists (AAPS) and the recipient of AAPS Regulatory Science Achievement Award, and University of Wisconsin Pharmaceutical Analysis Excellence Award. In addition, Dr. Nasr is a recipient of numerous US Government awards.