Discover who we are, scientific innovation at heart
We combine scientific expertise with strategic insight to deliver customized solutions that meet the unique needs of each project.
100+
ANDA
50+
Years Of Experience
25+
NDA
400+
Bioequivalence studies
50+
GMP audits


Tailored Services, designed especially for you (Product Development)

Formulation development
Comprehensive analysis of drug properties to design optimal formulations, ensuring stability and bioavailability.

Clinical development
Design robust Clinical trials, pharmacokinetics, bioequivalence studies

Medical writing
Protocal preparation, ICF preparation. Clinical study reports, Patients narratives,Orphan drug report

Regulatory Services

Regulatory
Crafting tailored strategies to ensure compliance with global regulatory standards, streamlining your path to market.

Dossier preparation
Preparation of CTD & e-CTD dossiers

Licenses and Approvals
EC approval

