Pharma Services Category of Eurofins CDMO

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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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Eurofins CDMO offers services during the whole development process and manage impurities synthesis and control.

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Eurofins CDMO has considerable experience with process development, successfully introducing hundreds of chemical steps to cGMP scale up and advancing several API’s to commercialization.

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Eurofins CDMO is experienced with the development and validation of several molecule API processes that are in various stages of regulatory approval across the globe.

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Combining process chemistry expertise with analytical solutions for your program, Eurofins CDMO provides API development services and commercialization support through the all process.

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Eurofins CDMO has expanded its capabilities through Solid State Research and Development (SSRD) services in support of API developmental programs.

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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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Eurofins CDMO team has considerable experience with process development, successfully introducing hundreds of chemical steps to cGMP scale up and advancing several API’s to commercialization.

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Eurofins CDMO provides integrated, end-to-end drug development solutions supporting clients from the earliest phases of API research and development through finished products.

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Eurofins CDMO provides integrated, end-to-end drug development solutions supporting clients from the earliest phases of API research and development through finished products.

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Eurofins CDMO offers integrated development services through the entire drug product life cycle, from highly potent active pharmaceutical ingredients (HPAPI) forward.

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Eurofins CDMO offers integrated development services through the entire drug product life cycle, from highly potent active pharmaceutical ingredients (HPAPI) forward.

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Eurofins CDMO offers integrated development services through the entire drug product life cycle, from highly potent active pharmaceutical ingredients (HPAPI) forward.

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We offer the complete portfolio of cell banking services, with the manufacture of Master and Working Cell Banks or End-of-Production Cell Banks under cGMP.

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Eurofins CDMO delivers solutions to its customers for the development and biomanufacturing of a broad range of biological molecules and product types (antibodies, proteins, enzymes, vaccines...).

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Eurofins CDMO has experience with a wide range of different drug delivery routes, drug delivery systems and drug production technologies.

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Eurofins CDMO has state-of-the art facilities for GMP compliant clinical supply manufacturing, packaging and labeling of liquid, semi-solid and solid dosage forms on lab and pilot scale for biologics.

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Eurofins CDMO offers integrated development services through the entire drug product life cycle, from highly potent active pharmaceutical ingredients (HPAPI) forward.

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Eurofins CDMO can to help you in: formulation transition from liquid to freeze dry form, solubilization & formulation study for injection, freeze drying cycle development & optimization.

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The Eurofins CDMO teams are highly experienced in the development of all galenic form. Powder or liquid, using water, non-aqueous phases and available solvants for sterile administration.

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The Eurofins CDMO teams are highly experienced in the development of all galenic form. Powder or liquid, using water, non-aqueous phases and available solvants for sterile administration.

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The Eurofins CDMO teams are highly experienced in the development of all galenic form. Powder or liquid, using water, non-aqueous phases and available solvants for sterile administration.

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The Eurofins CDMO teams are highly experienced in the development of all galenic form. Powder or liquid, using water, non-aqueous phases and available solvants for sterile administration.

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We offer drug development services encompassing preclinical development, formulation screening and development of liquid dosage forms for oral, nasal, parenteral and ophthalmic delivery.

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We offer drug development services encompassing preclinical development, formulation screening and development, analytical development of semi solid dosage forms for skin, mucosal or oral delivery.

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We offer a full suite of drug development services encompassing preclinical development, formulation screening and development, analytical development of solid dosage forms for oral delivery.

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We offer a full suite of drug development services encompassing preclinical development, formulation screening and development, analytical development of solid dosage forms for oral delivery.

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We offer a full suite of drug development services encompassing preclinical development, formulation screening and development, analytical development of solid dosage forms for oral delivery.

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Eurofins CCDMO can provide the primary packaging services of non-sterile solid forms (capsules and tablets) in HDPE bottles or blisters and in class C rooms.