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Our contract services group helps companies turn their new drug ideas into reality. Whether for phase I, phase II, phase III, or toxicology studies, we specialize in developing new synthetic routes while providing all necessary support to ensure regulatory compliance.

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Uquifa offers the opportunity to manage the development activities of any drug life cycle by offering services on DMF/CTD/COS application, stability studies, process validation and analytical method validation, working standard supply or impurity

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Maithili undertakes custom synthesis of key intermediates and active substances for innovator companies worldwide. We have the expertise in synthesizing diverse classes of molecules and offer gram to ton quantities in a cost-effective manner.

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Building on our experience of API development we can supply reference standard impurities, metabolites and related research materials. Using our supply chain network we generally source advanced intermediates to facilitate rapid and cost effective supply of these materials

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KriSan Biotech is capable to supply reference standards (including impurities) for customers and USP/EP/JP.

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Cerbios provides a full range of analytical services, including methods development and validation, analytical testing and release, stability studies, regulatory CMC documentation services and Reference standard characterization.

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In-house, ChemCon can synthesize, purify, characterize, qualify and certify your reference standard. ChemCon combines the expertise and facilities of an analytical service provider with those of a research and manufacturing organization.

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Dalton’s Custom Synthesis and Fine Chemical services offers a wide range of experience in the synthesis of low volume, high value small molecules for biotechnology and pharmaceutical applications.