Eurofins CDMO

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DMPK

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

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Pharma Service: API & Drug Product Development

Category: Preformulation & Material Science

Sub Category: PK / PD / TK

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API DEVELOPMENT & CONTRACT MANUFACTURING

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Eurofins CDMO provides API technology development services for the scale-up of complex small molecules with biotechnology and pharmaceutical applications including more potent APIs (HPAPIs) and cytotoxic compounds.

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Pharma Service: API & Drug Product Development

Category: API Development

Sub Category: Overview

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API DEVELOPMENT & VALIDATION

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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. Their cGMP units are equipped with cryogenic, hydrogenation & chromatography capabilities.

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Pharma Service: API & Drug Product Development

Category: API Development

Sub Category: Overview

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API COMMERCIALIZATION SUPPORT

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Combining process chemistry expertise with analytical solutions, Eurofins CDMO provides Active Pharmaceutical Ingredient (API) development services, route scouting & commercialization support to pharma companies.

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Pharma Service: Sales, Marketing, Registration

Category: Active Pharmaceutical Ingredients

Sub Category: France

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SOLID STATE

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Through the integration of synthetic process R&D, solid state R&D, preformulation and formulation development, Eurofins CDMo offers a knowledge-based quality-by-design approach throughout the API development and manufacturing.

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Pharma Service: API & Drug Product Development

Category: Preformulation & Material Science

Sub Category: Solid State Characterization

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FATE & PURGE SERVICES

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Eurofins CDMO has 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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Pharma Service: API & Drug Product Development

Category: API Development

Sub Category: Overview

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IMPURITY SYNTHESIS

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Eurofins CDMO identifies, isolates & synthesizes process related impurities to support process development, analytical control & regulatory requirements. They offer services for the whole drug development process & manage impurities synthesis & control.

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Pharma Service: API & Drug Product Development

Category: API Development

Sub Category: Impurity / Reference Standard

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PROCESS DEVELOPMENT & OPTIMIZATION

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Eurofins CDMO has a high degree of expertise process development, successfully introducing hundreds of chemical steps to cGMP scale up and advancing several APIs from route scouting through to commercialization.

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Pharma Service: API & Drug Product Development

Category: Formulation Development

Sub Category: Process Development & Optimization

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API DEVELOPMENT PROCESS OPTIMIZATION

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Eurofins CDMO team has considerable experience with process development, cGMP scale up & advancing several API’s to commercialization. It performs different CDMO services such as process optimization, analytical method development, stability studies, etc.

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Pharma Service: API & Drug Product Development

Category: API Development

Sub Category: Process Development & Optimization

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