Six decades of API expertise, a DSIR-recognised R&D centre and a USFDA / EU-GMP / WHO-PQ approved site — combined into a reliable CDMO partner for custom development and manufacturing.
Dedicated development and manufacture of Active Pharmaceutical Ingredients to your specifications, under strict confidentiality.
Route selection, process development and cost, yield and impurity optimization at our DSIR-recognised research centre.
Method development and validation, impurity profiling and ICH stability studies backed by modern instrumentation.
Seamless lab → pilot → commercial scale-up, backed by 2,400 MTPA of multipurpose manufacturing capacity.
DMF, CEP and dossier support for USFDA, EU-GMP, WHO-PQ and other regulated markets, drawing on a strong filing track record.
Synthesis, isolation and characterization of impurities, metabolites and reference standards for your analytical needs.
Tell us about your requirement and our team will get back to you with a confidential, tailored proposal.
Talk to our team