Bioequivalence CRO · Pune, India

Quality generics are a must, not an option.

Regulatory-compliant BA/BE studies that get your generics to market on time and on budget.

What we do

Built for bioequivalence.

One partner for your generic's whole journey to market, from bioanalysis and clinical conduct to regulatory submission.

01 · Centrifugation Plasma separated from every volunteer sample
02 · Sample preparation Standards, QCs and samples processed in 96-well format
03 · LC-MS/MS Drug concentrations quantified against an internal standard
100+ Man-years of experience
130+ Studies completed
100+ Clinical sites across India
0 USFDA 483 observations

Let's bring your generic to the market, together.

We are just an email away to give you a steady hand in your effort to bring your product to the market.