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iVRS News
Successfully completed USFDA Inspection of our Analytical Laboratory
Executed 360-Participant clinical study in Pain Management
Completed Atopic Dermatitis clinical study for Health Canada, leading to successful regulatory approval.
Successfully executed Phase I NCE Clinical Study
Successfully completed Sevelamer Carbonate API sameness study for TGA.
Executed NG and G-Tube studies for Health Canada and USFDA, with successful regulatory approval from both agencies
Completed 250+ Extractable & Leachable Studies
Showing Slide 1 of 7: Successfully completed USFDA Inspection of our Analytical Laboratory

Dr. D Prabakaran M.Pharm, Ph.D

Sr. Vice President – Technical Operations

Dr. Prabakaran is doctorate in pharmaceutical sciences from Dr. Hari Singh Gour University, Sagar, MP, and he started his career as formulation scientist in 2004. In 2006, he moved into clinical research and served generic pharmaceutical industry for 15 years in the area of formulation sciences, bioequivalence, late phase clinical studies, biopharmaceutics, in vitro-in vivo correlation, biostatistics, in vitro bioequivalence studies, clinical studies of derma, ophthalmic & pulmonary products, analytical and bioanalytical sciences.

His experience with respect to clinical research/in vitro studies entirely with regulated market like US, Europe, Australia, etc., and faced various regulatory audits. He is well versed with the regulatory expectations and up to date with regulatory guidance and newer approaches on generic drug development.


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