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We perform analytical development activities involving method development, impurities & degradation identification, compendial method verification, fate and purge studies etc.

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Pierre Fabre CDMO offers its customers the development and production of monoclonal antibodies and ADCs as well as toll manufacturing of injectable products (cytotoxic agents, monoclonal antibodies, ADCs, vaccines, etc.)

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LEBSA offers an end-to-end partnership for custom API development, scale-up and manufacturing with a flexible multipurpose EU GMP Pilot Plant, from grams to tones, with a client centric approach.

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An offer complying with Good Manufacturing Practices (GMP), closely monitored by the Quality Insurance and Regulatory Affairs services: Laboratory, Kilolab, Pilot, industrial production and preparatory chromatography services.

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Biophore, an established pharmaceutical company, is engaged in the development and manufacturing of niche pharmaceutical products for the generic industry. Biophore has emerged as a trusted partner in the generic industry across US, Europe and other regulated markets.

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Eurofins CDMO's development team operates well-equipped laboratories to handle the most complex API development challenges.

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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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Equipped with a recognized and certified manufacturing base, we provide the full range of our expertise to carry out in the fields of pharma and non-pharma active ingredients, injectables and monoclonal antibodies, dry forms and non-sterile liquids.

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Zach has over 30 years of experience in multi-step syntheses involving complex reactions.We have dedicated R&D and analytical development teams on each site, and state-of-the art analytical equipment.

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Biospectra provides custom API Development with various supports like Analytical support, Development Support and other supports through the life of your product.

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Sequent has invested in facilities with an objective of creating an integrated, flexible unit capable of manufacturing several niche & complex APIs. The manufacturing facalities are capable of meeting the growing demand of our key products in the USFDA and WHO regulated markets.

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Our contract micronization services have been refined and improved based on actual in-depth experience gained from our daily processing operations. Our state-of-the art material handling service applies micronization technology based on this combination of improved equipment and practiced,

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Kimia Biosciences' strength lies in focus on R & D where we propose to continuously invest and innovate to be in line with the global technological advancements and offer most cost effective processes to our pharmaceutical fraternity in our country as well as globally.

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Equipped with a recognized and certified manufacturing base, we provide the full range of our expertise to carry out in the fields of pharma and non-pharma active ingredients, injectables and monoclonal antibodies, dry forms and non-sterile liquids.

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Eurofins CDMO has a strong experience in impurity control strategy from IND through to commercial stages and have demonstrated track-record in the design and execution of fate and purge studies.

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Pierre Fabre CDMO offers its customers the development and production of monoclonal antibodies and ADCs as well as toll manufacturing of injectable products (cytotoxic agents, monoclonal antibodies, ADCs, vaccines, etc)

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Eurofins CDMO is experienced with the development & validation of several molecule API processes that are in various stages of regulatory approval across the globe. Our cGMP units are equipped with cryogenic, hydrogenation, & chromatography capabilities.

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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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Delivering reliable and scalable crystallization processes through market leading capabilities and technologies in engineered API particle characterization.

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R&D center is located in High-tech park of Shanghai with area about 1,000 square meters. It is equipped with chemical synthesis room, formulation room and advanced instrument room. What’s more, there are 5 professionals focusing on new drug development.

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R&D center is located in High-tech park of Shanghai with area about 1,000 square meters. It is equipped with chemical synthesis room, formulation room and advanced instrument room. What’s more, there are 5 professionals focusing on new drug development.

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R&D center is located in High-tech park of Shanghai with area about 1,000 square meters. It is equipped with chemical synthesis room, formulation room and advanced instrument room. What’s more, there are 5 professionals focusing on new drug development.

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Dedicated laboratory and infrastructure addressing the needs of clients with highly potent synthetic molecules including containment solutions for beta-lactams.

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Dedicated laboratory and infrastructure addressing the needs of clients with highly potent synthetic molecules including containment solutions for beta-lactams.

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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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Grace's talented team of experts supported by a comprehensive cGMP environment, help customers in the pharmaceutical, nutraceutical, food and beverage, chemical processing, and other industries solve their most complex challenges.

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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.

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Pfanstiehl is a global leader in the manufacture of cGMP-produced, high purity, injectable grade excipients and bioprocessing solutions.