Efficient, Cost Effective & Safe manufacturing process development.
- API Development
- KSM and Intermediates Development
- Nutraceuticals Development
- Impurity Synthesis & Isolation
CRO,CRAMS, & CDMO to support generic and new drug development.
Drug Discovery – NCE Synthesis
CMC for Pre-clinical & Clinical stages (cGMP)
Safety Study/ Evaluation
QSAR (Quantitative Structure–Activity Relationship) and Genotoxic Evaluation for Regulatory Submission
Production and characterization of high-quality reference materials to support regulatory submissions and global compliance.

Technical Capabilities Chemical R&D