Khan, Mansoor individual record
Professor and Vice Dean
overview

Dr. Mansoor A. Khan serves as a professor and Vice Dean of the Texas A&M University Rangel College of Pharmacy at College Station, Texas. Prior to joining Texas A&M in 2015, he served as the Director of Product Quality Research and a Senior Biomedical Research Scientist (SBRS) at CDER in US Food and Drug Administration for over eleven years. In FDA, he led the research and review teams to promote manufacturing science, and served as a founding member of the FDA Emerging Technology Team. Dr. Khan received his Ph.D. degree in industrial pharmacy form St. Johns University in NY. He has published over 335 peer-reviewed manuscripts in pharmaceutical formulations and manufacturing sciences, and delivered over 300 presentations world-wide. Dr. Khan's research, currently supported by the NIH and FDA, spans drug delivery and formulations, and he has received over ten million dollars in funding as a principal investigator.



Dr. Khan has held leadership positions at the AAPS including elected chair of formulations design and development (FDD) section. He serves on the editorial board of Pharmaceutical Technology, International Journal of Pharmaceutics, AAPSPharmsciTech, and the Drug Delivery and Translational Research. He has received about 20 FDA/CDER review, research, and exemplary achievement awards, outstanding alumni award at St. Johns University College of Pharmacy, Excellence Award in Texas A&M University. He received the 2012 AAPS Research Achievement Award in Formulations Design and Development. He is also an AAPS and AAiPS Fellow. Dr. Khan served as FDA representative to the World Health Organization (WHO), United States Pharmacopoeia (USP), European Medicine Agency (EMA), DARPA, NIH, National Institute of Pharmaceutical Technology and Education (NIPTE), and International Pharmaceutical Federation (FIP). He is also a member of the European Union Academy of Sciences.

education and training
selected publications
Academic Articles323
  • Helal, N. A., Martinez, M. N., Longstaff, D. G., Rahman, Z., Nutan, M., & Khan, M. A. (2024). Development and Validation of Matrix of Chemistry, Manufacturing, and Control (MoCMC) System for Intramammary Drug Products (IMM).. Pharmaceutical Research. 41(5), 1007-1020.
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  • Kayalar, C., Helal, N., Mohamed, E. M., Dharani, S., Khuroo, T., Kuttolamadom, M. A., Rahman, Z., & Khan, M. A. (2024). In Vitro and In Vivo testing of 3D-Printed Amorphous Lopinavir Printlets by SelectiveLaser Sinitering: Improved Bioavailability of a Poorly Soluble Drug.. 25(1), 20.
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  • Dharani, S., Mohamed, E. M., Rahman, Z., & Khan, M. A. (2024). Patient In-Use Stability Testing of FDA-Approved Metformin Combination Products for N-Nitrosamine Impurity.. AAPS PharmSciTech. 25(1), 19.
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  • Kayalar, C., Rahman, Z., Mohamed, E. M., Dharani, S., Khuroo, T., Helal, N., Kuttolamadom, M. A., & Khan, M. A. (2023). Preparation and Characterization of 3D-Printed Dose-Flexible Printlets of Tenofovir Disoproxil Fumarate.. AAPS PharmSciTech. 24(6), 171.
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  • Mohamed, E. M., Dharani, S., Khuroo, T., Hamed, R., Khan, M. A., & Rahman, Z. (2023). In Vitro and In Vivo Characterization of the Transdermal Gel Formulation of Desloratadine for Prevention of Obesity and Metabolic Syndrome.. Pharmaceuticals. 16(4), 578-578.
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Books2
  • Reddy, I. K., & Khan, M. A. (2017). Essential Math and Calculations for Pharmacy Technicians. Taylor & Francis.
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  • Kahn, M. A., & Reddy, I. K. (2000). Pharmaceutical and Clinical Calculations, 2nd Edition. CRC Press.
Chapters31
  • Charoo, N. A., Mohamed, E. M., Kuttolamadom, M., Khan, M. A., & Rahman, Z. (2023). Binder Jetting Powder Bed 3D Printing for the Fabrication of Drug Delivery System. Nano- and Microfabrication Techniques in Drug Delivery. 137-172. Springer Nature.
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  • Awotwe-Otoo, D., & Khan, M. (2019). Regulatory Aspects of Freeze-Drying. Lyophilization of Pharmaceuticals and Biologicals. 173-192. Springer Nature.
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  • Rahman, Z., Charoo, N. A., Akhter, S., Beg, S., Reddy, I. K., & Khan, M. A. (2018). Chapter 16 Nanotechnology-based drug products Science and regulatory considerations. Nanoscale Fabrication, Optimization, Scale-Up and Biological Aspects of Pharmaceutical Nanotechnology. 619-655. Elsevier.
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  • Mockus, L., LeBlond, D., Reklaitis, G. V., Basu, P. K., Paul, T., Pease, N., Nail, S. L., & Khan, M. A. (2017). Design Space Definition. Reklaitis, G. V., Seymour, C., & Garcia-Munoz, S. (Eds.), Comprehensive Quality by Design for Pharmaceutical Product Development and Manufacture. 301-318. Wiley.
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  • Wu, H., & Khan, M. A. (2017). Quality by Design. Reklaitis, G. V., Seymour, C., & Garcia-Munoz, S. (Eds.), Comprehensive Quality by Design for Pharmaceutical Product Development and Manufacture. 235-256. Wiley.
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Conference Papers27
  • Funkhouser, C., Ali, S., Richardson, L., Rahman, Z., Khan, M., & Kuttolamadom, M. (2020). THERMAL INFLUENCE ON PRINTLET QUALITY IN THE SELECTIVE LASER SINTERING OF PHARMACEUTICAL FORMULATIONS. Volume 1: Additive Manufacturing; Advanced Materials Manufacturing; Biomanufacturing; Life Cycle Engineering; Manufacturing Equipment and Automation.
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  • Mohammed, E., Hamed, R., Barakh Ali, S. F., Khan, M. A., Ozkan, T., Kuttolamadom, M., & Rahman, Z. (2020). Chemometric Assisted X-Ray Powder Diffractometry Method for Crystalline Lopinavir Quantification in 3D Printlets Manufactured by Selective Laser Sintering. 2020 AAPS Annual Meeting.
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  • Khan, M. A., Wu, K., & Gupta, A. (2012). FDA: contribution to developing pediatric formulations and transatlantic collaboration.. International Journal of Pharmaceutics. 435(2), 146-148.
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researcher on
Email
mkhan@tamu.edu
First Name
Mansoor
Last Name
Khan