Premium Intermediates
& Key Starting Materials
cGMP-certified supplier of high-purity pharmaceutical intermediates. Complete DMF dossiers, CEP filings, and global regulatory compliance. Longterm partner for bulk APIs and key starting materials.
βοΈ Quality at Every Step
Our intermediates and APIs are synthesised with the utmost precision and undergo rigorous quality checks β purity levels that exceed international benchmarks across IP, BP, USP, and EP pharmacopoeias.
π Regulatory Excellence
Manufacturing processes adhere to ICH Q7 GMP guidelines, certified by CDSCO, WHO-GMP, PMDA, and ISO. DMF dossiers available for USA (USFDA), Europe (CEP), Korea (KDMF), Japan (JDMF), and Brazil (ANVISA).
π Reliable Global Supply
Consistent, uninterrupted supply to pharmaceutical manufacturers across 80+ countries. Custom synthesis and long-term contract manufacturing available as per client specifications and process requirements.
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