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Quraxia provides complete Active Pharmaceutical Ingredient (API) development and custom synthesis services, ensuring regulatory compliance and scalability from lab to commercialization.
Our Expertise
Route design & process development
Analytical method development (HPLC, LCMS, NMR)
GMP-compliant scale-up & validation
Development of oncology APIs, peptides, hormones, high-potency molecules
Our Process
Discovery & route scouting → optimized synthesis design
Pilot studies → scale-up verification
Validation → robust quality assurance
Tech-transfer → seamless transition to manufacturing
Our Haridwar R&D center supports not just API development, but also formulations, analytical protocols, and regulatory validation, making Quraxia a one-stop solution from molecule to market launch.
