Ziyaur Rahman did his B.S. in Pharmacy (2000) and M.S. in Pharmaceutics (2002) from Hamdard University, New Delhi, India. He did his Ph.D. in Pharmaceutics (2005) from Hamdard University, New Delhi, India. He completed his Postdoctoral Research Associate (2007-2008) from University of Mississippi.

Formulation and process design of traditional (tablet, capsule, gel, emulsion, ointment etc) and complex dosage forms (microparticles, implant, pediatric, nanosuspension, nanoemulsion etc.); Drug product quality and process understanding through Quality by Design (QbD) and Process Analytical Technologies (PAT) approaches; Development of in vitro release performance tests for traditional and complex dosage forms; Evaluation of in-vitro bioequivalence for complex dosage forms; Design and evaluation of abuse-deterrent/meth-deterrent formulations; 3-dimensional printers’ application in pharmaceuticals printing; Continuous manufacturing of pharmaceutical dosage forms; Application of non-destructive methods (Raman, FTIR, XRPD, ssNMR, NIR, NIR-Chemical imaging) for quantification of components of formulations; Multivariate analysis (chemometrics, PCR, PLSR, DFA etc.) in pharmaceutics