Fill & Finish
Unlock the potential of your sterile Fill & Finish projects with our comprehensive solutions tailored into clinical trials.
One-stop-shop for Fill and Finish
Our complete Fill and Finish service chain for Drug Products includes :
- Formulation
- Aseptic Fill and Finish GMP certified
- Visual inspection
- Sterility testing
- Labelling
- Packaging and Qualified Person certified Release
Why choose our Fill & Finish service?
1. Safety Assured
Our end-to-end Fill & Finish solution guarantees safety at every step of the biopharmaceutical journey. From early R&D to aseptic filling compliant with GMP standards for pre-clinical and clinical phases, we adhere to Annex 1 criteria, ensuring the highest level of safety and regulatory compliance.
2. Flexibility Unleashed
With fill volumes of up to 25 liters, accommodating the filling of up to 500 vials per series, we offer unparalleled flexibility. Choose from a range of container sizes, from 0.5mL to 50mL, tailored precisely to your project’s needs.
3. Customized Excellence
Our Fill and Finish service caters to a diverse array of active pharmaceutical ingredients (APIs). Whether it’s small molecules, amino acids, peptides, proteins, or monoclonal antibodies, our solution delivers reliability and efficiency, meeting your specific requirements with precision.
Let’s Collaborate
Ready to ensure the success of your preclinical and clinical trials?
Entrust your Fill and Finish projects to us, and let our expertise drive you towards your objectives.
Schedule a personalized meeting to discuss your unique requirements and explore how our solutions can accelerate your journey to market success.
+33(0) 5 61 28 70 75
End-to-end Fill & Finish solutions for injectable pharmaceuticals
Tailored excellence for your sterile vial filling projects
As a world-class CDMO expert, we specialize in providing sterile aseptic filling services for a wide spectrum of APIs and vectors.
Our adherence to global GMP-compliance standards ensures that your drug products meet exact specifications, facilitating seamless progression through preclinical and clinical trials.
Tailored API Solutions for Seamless Development
Whichever API you choose, we ensure a smooth and efficient development phase with rapid project onboarding.
Our team is committed to minimizing delays and accelerating your timeline. With flexible batch sizes various vial options, we can quickly supply up to 500 vials, meeting your project’s needs promptly and effectively.
State-of-the-Art Equipment:
We take pride in our equipment, meticulously selected to adhere to Annex 1 standards (EU guidelines for GMP of sterile medicinal products for human and veterinary use).
Each piece undergoes rigorous quality control measures, eliminating open phases and significantly reducing the risk of contamination. Our facilities boast:
- 1 autonomous production area
- Aseptic filling under grade A conditions
Get in Touch
Ready to transform your Fill & Finish projects into reality?
Contact us today to arrange a personalized consultation and discover how our cutting-edge solutions can elevate your biopharmaceutical endeavors.
+33(0) 5 61 28 70 75
WORLD-CLASS CGMP MANUFACTURING FACILITY
Our facilities are fully compliant with both American and European GMP guidelines, ensuring the highest standards of quality and safety for your therapeutic products.