Drug development and manufacturing for biologics and small molecules, with integrated services from preclinical, clinical to commercial.

Our services

Comprehensive details of our services, methods and offerings can be found on our global website using the information below.

Why Eurofins CDMO

Scientific expertise

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With over two decades of expertise, we deliver integrated drug development and manufacturing services, ensuring seamless pathways for your programme from preclinical to commercialisation.

Diverse programmes, flexible CDMO

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We are proud to serve a diverse range of clients, from early-stage startups to pharmaceutical companies, providing individualised, flexible and high-quality service to all.

Integrated, customised solutions

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Currently manufacturing several API (Active Pharmaceutical Ingredient) products, we combine expertise in small molecules, biologics, and ADCs with specialised services designed to de-risk and accelerate product development.

Strong quality and management systems

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Underpinned by a strong quality and project management system, our team of experts navigate complex regulatory compliance within quality frameworks with a focus on timeline, budget and communication.

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