Our biomanufacturing services

Eurofins CDMO offers a comprehensive suite of solutions to empower your biologics journey. Our state-of-the-art R&D laboratories and GMP-compliant cleanroom facilities enable us to support your projects from early-stage development to clinical supply manufacturing

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Freeze drying services

When it comes to biopharmaceutical development, stability is paramount. At Eurofins CDMO, we recognise the significance of scalability and commercial viability in achieving lasting stability. Our sterile manufacturing service portfolio encompasses cutting-edge development laboratories featuring state-of-the-art freeze dryers.

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Our specialised services:

  • Formulation transition: seamlessly shift from liquid to freeze-dry form, ensuring enhanced stability and sustainability.
  • Optimised freeze drying / lyophillization services: streamline processes and reducing costs while optimising freeze drying cycle.
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Sterile biomanufacturing services

Eurofins CDMO presents an array of aseptic processing services that cater to diverse drug product configurations. With flexibility to accommodate a wide range of compounds, primary packaging systems, batch sizes, and fill volumes, we are your strategic partner for both clinical trials and commercial use. Our sterile aseptic filling activities adhere to GMP-compliance standards, ensuring your biologics to meet all the regulatory requirements.