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Bachem's cGMP Production Capabilities includes Process Development, Solution Phase Peptide Synthesis, Solid Phase Peptide Synthesis (SPPS), Cleavage from the Resin Purification, Preparative HPLC, In-Process Control, Freeze Drying, Small Molecules, etc

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Malladi provides reliable manufacturing capabilities for the production of a wide range of APIs & intermediates. Our GMP compliant manufacturing facilities are state-of-the- art facilities approved by USFDA.

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Gentec Pharmaceutical Group offers API, intermediates and HPAPIs developments and manufacture in our plants, Duke Chem and Pharmanoid, under contract manufacturing.

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The GMP operating pilot is equipped with a double enamel line (up to 800 lt) and a steel line (up to 1000 lt), two centrifuges and rectification capacity (stainless steel) in full and in vacuum.

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Our API manufacturing facility is focused on manufacturing semi-synthetic based API’s with fermentation capacity of more than 500m3. The site practices cGMP and inspected by global regulatory agencies like USFDA, EUGMP, Japanese AFM, and Indian State GMP.

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At our Center of Excellence for Semi-solids and Liquids in San Antonio, 400 professionals provide cGMP manufacturing support for drugs at pilot, clinical and commercial scales.