Empower your drug development with our formulation expertise
Eurofins CDMO offers a comprehensive suite of solutions to empower your biologics journey. Our state-of-the-art R&D labs and GMP-compliant cleanroom facilities enable us to support your projects from early-stage development to clinical supply manufacturing.
Our expertise
We are experts in innovative formulations that optimize stability and bioavailability. We offer solutions for solid and liquid dosage forms, accommodating proteins, antibodies, peptides, live biotherapeutic products, plasmid DNA and oligonucleotides. These tailored formulations can be designed for various delivery routes, including parenteral, oral, nasal, and ophthalmic administration. Eurofins CDMO partners with you to deliver preclinical and early-phase clinical trial materials in the most adapted dosage forms, from sterile to non-sterile batches.
Formulation screening services
Formulation screening is performed in function of drug product development and administration route. Different type of buffers and excipients will be tested in order to stabilize the drug substance taking into account the needs for the applied delivery route. Information gathered during pre-formulation screening will speed up this process. The different drug delivery concepts are selected and compared to one another in terms of stability, efficacy and feasibility. Eurofins CDMO has experience with a wide range of different drug delivery routes, drug delivery systems and drug production technologies.
Your benefits
- Dosage forms and administration routes adapted to your patient needs from sterile parenterals to oral solutions
- Strong background in freeze-drying from R&D to scale-up and manufacturing
- Integrated and comprehensive analytical support from early development phases
- Seamless process transition from R&D to GMP manufacturing
