Find the capability tailored to your clinical needs
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 non sterile biomanufacturing services
- Freeze drying
- Spray drying
- Wet granulation
- Dry granulation
- Bead layering
- Tablet manufacturing
- Capsule encapsulation/over-encapsulation
- Microsuspensions
Freeze drying services
In the realm of pharmaceutical development, stability is paramount. Many APIs face instability in aqueous phases, necessitating meticulous galenic studies to ensure prolonged stability. At Eurofins CDMO, we recognize the significance of scalability and commercial viability in achieving lasting stability. Our sterile manufacturing service portfolio is designed to elevate your API's stability, driving it to a higher stage of performance. With cutting-edge development laboratories featuring state-of-the-art labscale freeze dryers, we embark on a journey to reshape drug stability.
Our specialized services:
- Formulation Transition: Seamlessly shift from liquid to freeze-dry form, ensuring enhanced stability and sustainability.
- Solubilization and Formulation Study: Unlock the potential of injection-ready formulations, enhancing efficacy and safety.
- Optimized Freeze Drying: Streamline processes, reducing costs while optimizing freeze drying cycles.
- Cycle Development: Meticulously craft freeze drying cycles to ensure impeccable stability.
Our 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 in transforming your Active Pharmaceutical Ingredient or bulk product into Finished Dosage Forms for both clinical trials and commercial use. Our sterile aseptic filling activities adhere to GMP-compliance standards, ensuring your biologics to meet all the requirements.
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