Molkem delivers high-quality Active Pharmaceutical Ingredients (APIs) from WHO-GMP, ANVISA, EU GMP, and USFDA-approved facilities. We specialize in tailored API solutions, offering flexibility from small-batch to large-scale production while adhering to the highest global regulatory standards. 

Our end-to-end regulatory support includes DMF filings (CEP, US-DMF, CADIFA), Tech Packs, Stability Studies, and strict compliance with pharmacopeial quality parameters ensuring seamless integration into your pharmaceutical processes. 

With a strong commitment to responsible sourcing, full traceability, and patent non-infringing routes, we enable our customers to bring products to market faster and with greater confidence. At Molkem, quality, transparency, and customer satisfaction are at the heart of our operations, making us your trusted partner in the global pharmaceutical supply chain.