We offer an extensive array of development services encompassing both chemical and formulation development. Beginning from pre-clinical and clinical trials, we specialize in synthesizing and manufacturing new drug candidates.
We provide a wide range of scalable, flexible and reliable services and capabilities at each phase of drug lifecycle.
Our capabilities range from producing small quantities, typically in grams, for efficacy and toxicology studies, to scaling up to multi-kilogram quantities for clinical trial investigations.
Our experienced development and manufacturing expertise, robust infrastructure and skilled team provide a strong foundation for rapid scale-up and delivery of key milestones for your contract development and manufacturing program.
Innovative Route of Synthesis (ROS) establishment from concept to sustainable process.
Phase-appropriate process development for successful scale-up, ensuring timely delivery for clinical trials.
Rigorous Process Safety evaluation with data-driven EHS assessment.
Full range of stability services across different time zones.
Phase-appropriate development and manufacturing for pre-clinical and Phase-I NCEs, meeting regulatory compliance from process development to commercial batch production.
WHO and State GMP-approved sites ensuring international quality standards
From early discovery to commercialization including molecule development, regulatory, formulation, and purification expertise
Strong expertise, experience,, and technology in complex chemistry.
With an R&D; center, 3 Production blocks, well-equipped QC labs, 400 MT capacitated warehouse with specialized areas
Comprehensive information security coverage with backup and business continuity plans.
Structured assurance and governance measures ensure business continuity.
A powerful team of 12+ highly experienced and expert scientists and 200+ trained and skilled employees
Committed to the highest ESG standards