Eurofins CDMO India, is your dedicated partner in accelerating your drug substance journey, from early-phase development to commercial supply. We offer a complete suite of services designed to streamline your process development & manufacturing needs: 1. GMP manufacturing of regulatory starting materials (RSM) and clinical supplies 2. Expert synthesis, process development, and scale-up for preclinical studies 3. Comprehensive analytical development and robust stability-indicating studies Leverage our deep expertise and state-of-the-art capabilities to ensure your product moves efficiently through every drug development stage. Contact us - [email protected]