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.