Consultancy

We have more than 13 years of versatile experience in biostatistics, Bioequivalence, Clinical Trials, Dissolution similarity, Pharmacovigilance, IVIVC, Stability analysis, SAS programming.

PHARMA-STATS work with several pharmaceutical/CRO clients in India, USA & EU region on Clinical trial projects.

Expertise in CDISC solution for Bioequivalence FDA Submissions.