Dr. Mansoor A. Khan is the Director of Product Quality Research in the Center for Drug Evaluation and Research at the U.S. Food and Drug Administration (USFDA)
Prior to joining the USFDA, Dr. Khan was a Professor of Pharmaceutics and Director of the Graduate Program in the School of Pharmacy at Texas Tech University Health Sciences Center. He is a Registered Pharmacist and earned his Ph.D. in Industrial Pharmacy from the St. John's University.
He has published more than 135 peer-reviewed manuscripts; four texts, including Pharmaceutical and Clinical Calculations; five book chapters; and given more than 125 presentations at various meetings. He has been recognized as an AAPS fellow and serves on the editorial board of Pharmaceutical Technology, the Journal of Clinical Research and Regulatory Affairs and the journal Critical Reviews in Therapeutic Drug Carrier Systems.
Dr. Khan's research focus is primarily in the areas of quality by design and process analytical technologies, controlled drug delivery of challenging molecules, and the oral delivery of macromolecules and nano-particles.