Eurofins CDMO

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

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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