Research & Development
Key Capabilities
Our R&D division offers end-to-end contract research services, from early-stage development to dossier submission for global regulatory bodies.
Our Core Areas of Expertise:
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Formulation Development across therapeutic categories like anti-diabetic, cardiovascular, CNS, and antibiotics
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Bioequivalence & Bioavailability Studies in accordance with DCGI and international guidelines
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Scale-Up & Technology Transfer Support for commercial manufacturing
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Process Optimization and Technical Troubleshooting across manufacturing sites
Our R&D also provides strong regulatory support, including:
- Preparation of dossiers for ANDAs, NDAs, and global regulatory submissions
- Patent evaluations and filings
- Documentation for USFDA, bioequivalence samples, and commercial batches