The incumbent will be responsible for
Developing Bio-related media & evaluate in vitro profile.
Predict in-vitro, in-vivo correlation
Approve Pilot & Pivotal BE related Protocol based on in-vitro, in-vivo correlation result
Study critical analysis of important issues related to BA
Evaluate the date generated from in-vitro, in-vivo correlation software
Worked with the formulators for pharmacokinetics inputs during product development
Work with analytical team for development of discrepancy studies / discriminatory media.
M.Pharma . / Ph.D. with relevant experience in a reputed Pharma Company.
Must have knowledge regarding regulatory requirement on in-vitro, in- vivo studies & basic of Pharmacokinetics parameter that describe the fate of the drug in the body.