Mr. Walave is a B.Pharm. holds over 8 years of functional experience in pharmacokinetics, bioavailability/ bioequivalence studies, protocol, clinical study report and clinical study design.

He holds comprehensive experience at Synapse in various functions of handling end-to-end operations of Clinical Research Department. Mr. Walave also contributes in successful regulatory audits and inspections from leading regulatory bodies at Synapse.