Ziyaur Rahman is an Professor of Pharmaceutical Sciences at the Irma Lerma Rangel School of
Pharmacy, Health Science Center, Texas A&M University. He received his
Bachelor’s in Pharmacy and Master’s in Pharmaceutics from Hamdard
University. He earned his Ph.D. in Pharmaceutics from Hamdard University in
2005. His research interests lie in the formulation and process design of
traditional and complex dosage forms with focus on Quality by Design (QbD)
and Process Analytical Technologies (PAT). He has expertise in developing in
vitro release performance tests for traditional and complex dosage forms,
evaluating in vitro bioequivalence, and designing abuse-deterrent
formulations. He is also interested in the application of non-destructive
methods for quantifying components of formulations and multivariate analysis
in pharmaceutics.
Ziyaur Rahman is an Professor of Pharmaceutical Sciences at the Irma Lerma Rangel School of
Pharmacy, Health Science Center, Texas A&M University. He received his
Bachelor’s in Pharmacy and Master’s in Pharmaceutics from Hamdard
University. He earned his Ph.D. in Pharmaceutics from Hamdard University in
2005. His research interests lie in the formulation and process design of
traditional and complex dosage forms with focus on Quality by Design (QbD)
and Process Analytical Technologies (PAT). He has expertise in developing in
vitro release performance tests for traditional and complex dosage forms,
evaluating in vitro bioequivalence, and designing abuse-deterrent
formulations. He is also interested in the application of non-destructive
methods for quantifying components of formulations and multivariate analysis
in pharmaceutics.