Dr. Qureshi has extensive (30+ year) experience in conducting hands-on and multi-disciplinary laboratory research in pharmaceutical areas for regulatory assessment purposes while working with Health Canada. He is an internationally recognised expert in the areas of pharmacokinetics, biopharmaceutics, drug dissolution testing, analytical chemistry as related to characterization of pharmaceuticals, in particular based on in vitro (dissolution) and bioavailability/bioequivalence (humans and animals) assessments. At present, Dr. Qureshi provides teaching, training and consulting services, in the area of his expertise as noted above, for improved pharmaceutical products development and assessments.
Dissolution method development; In vitro-in vivo correlation (IVIVC); Sink condition; in vitro
-to- in vivo profiling (IVIVP); Convolution; Biopharmaceutic classification system