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Complete development of APIs, “building blocks” and impurities, in cooperation with and supervised by the interested party.

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Axyntis Group has expanded its offerings in fine chemicals and is able to handle projects from the gram to the ton, while complying with Good Manufacturing Practices (GMP) and maintaining high hygiene, security and quality standards.

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Drug’On Pharma Switzerland was the last company to be set up in the Orofino Pharmaceuticals Group. The Group bought out the ex Knoll and Abbott manufacturing site in Liestal,Switzerland. The chemical manufacturing site produces active pharmaceuticals ingredients (API) and intermediates.

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The Pharma & Chemical division is dedicated to research, development and production of active ingredients and synthetic intermediates – used for manufacturing active ingredients – on behalf of various industries and in compliance with good manufacturing practices (GMP).

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Siegfried offers experience and proficiency in the chemical and pharmaceutical industry. Siegfried is the ideal partner for both cGMP and non-cGMP intermediates.

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Shouyuan chemical specializes in manufacturing, supplying, and custom synsthesis latest chemicals. Our products cover all kinds of range like pharmaceuticals, agrochemicals, electronic chemicals, surfactants and other specialty chemicals.

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Alven is reliable partner for development, process optimization, scale-up and cGMP production of branded and generic API’s and intermediates.

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Our experienced process development chemists are an asset to our customers regardless of their size - virtual, small, mid-size, or large pharma/biotech. The scientists in the Flamma Italy R&D group and the Flamma Honkai R&D group provide optimal service to complete projects.

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At Cambrex, we use our experience and expertise to efficiently bring your small molecule intermediates and APIs from early clinical phase to commercial production.

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Ipochem represents experience and proficiency in the chemical and pharmaceutical industry. Technologies and capabilities include the development and production of APIs as well as physical operations of milling and micronization.

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Our team of experienced Scientists has expertise in the custom synthesis of a wide range of small molecules like API, stable isotope labeled compounds, chemical intermediates, drug metabolites, drug analogs, analytical standards, reference standards, pharmaceutical impurities.

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Servier brings 60 years of experience in process development, intermediates, APIs and high-potency APIs. Our full cGMP / FDAapproved chemistry network includes R&D, production and supply chain expertise with full regulatory support. Servier CDMO’s teams are able to follow your projects from

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Huvepharma® Italia is a recognized as a reliable supplier of development and manufacturing services of APIs & advanced intermediates for leaders in the international market.