Pharma Services Category of Eurofins CDMO

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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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Our team of highly qualified scientists in Solid State Science (material science, formulation) offer the services such as Polymorphism & crystallinity study (PXRD, DSC), API Solid Form Development, Pharmaceutical salt screening & development etc.

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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 identifies, isolates & synthesizes process related impurities to support process development, analytical control & regulatory requirements. We offer services during the whole development process & manage impurities synthesis & control.

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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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All type of APIs can be manufactured in our facilities where we developed specific expertise for the fill & finish of other liquid formulations than standard ones such as sterile powders, suspensions, sterile semi-solids etc.

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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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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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Eurofins Contract Development & Manufacturing Organization is your leading partner for specialized preclinical services for a complete IND/IMPD package that includes Drug Metabolism and Pharmacokinetic (DMPK) studies.

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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 also perform ICH compliant stability studies including stress studies, accelerated and long-term stability studies to support regulatory CMC programs and process development.

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To support API solid form R & D programs, we apply High-Throughput Screening Technology for discovery of new polymorphs, particle size engineering & development or automated crystallization scale-up development.

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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 also perform ICH compliant stability studies including stress studies, accelerated and long-term stability studies to support regulatory CMC programs and process development.

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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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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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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 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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Eurofins CDMO regulatory experts will draft, review and manage the necessary documents to enable the building of Common Technical Document (CTD) for product registration and life-cycle submissions.

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Eurofins Contract Development & Manufacturing Organization offers GMP storage of 560 m3 at 15-25°C,146 m3 at 2-8°C, 2.6 m3 at 20°C and 0.5 m3 at -80°C.

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Eurofins CDMO offers the skills & capability to prepare & review documents for clinical trial application (IND/IMPD). This includes manufacture & support for Phase I, II & III studies, IND/IMPD quality sections related to drug substance & drug product.

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Eurofins CDMO can perform customized labeling and secondary packaging of every clinical trial phases for sterile and non-sterile dosage forms (blisters, blister-cards, vials, syringes, bottles).