Welcome to a CDMO where science meets service excellence, where innovation merges with reliability
Revolutionise your clinical development with our expert development & manufacturing services for innovative biomolecules
We support your project from R&D to in-market supply
Start your CMC journey confidently with our tailored development and GMP manufacturing services
R&D services
Custom production services with all prominent expression systems providing recombinant proteins for your R&D studies.
Process Development
Developing top-tier manufacturing processes for a range of molecules: proteins, antibodies, bioconjugates, and nanodrugs.
Analytical Development
Phase-appropriate method development for mammalian, microbial, and bioconjugate manufacturing.
GMP Manufacturing
Our top-notch GMP facilities manufacture preclinical, clinical, and small commercial batches of innovative therapies.
Fill & Finish
Our in-house aseptic filling supports liquid drug product manufacturing, accelerating your path to clinic and market.
Project Management
From start to finish, our expert team of scientists guides you seamlessly through every step of your CMC journey.
Client stories: what they were looking for in a CDMO
We’ve helped our customers develop and manufacture innovative therapies for more than 20 years.
From R&D to commercial production: our expertise spans all stages of biotherapeutics development
Years as a CDMO
Years' expertise in aseptic filling
Clients served worldwide
Protein programmes managed
GTP Bioways – your partner for biologics development and manufacturing
Our process development and manufacturing facilities sit in the heart of Europe.
Saint-Julien
mAb & ADC GMP Manufacturing
Toulouse
Cell Line Development, GMP Manufacturing & Fill & Finish
Labège
Microbial & Mammalian Process Development
Veyre-Monton
HCP Risk Management & Immunoassays Development
From our blog:Our biologics CDMO experience
Aseptic Filling for Biologics: What to Know
What is aseptic filling? Key considerations for biologics Aseptic filling—often called aseptic fill-finish—is the final, high-stakes step that transfers a sterile drug product into a sterile primary...
How to Choose the Right CDMO for Your Biologics Program
How to Choose the Right CDMO for Your Biologics Program Selecting a Contract Development and Manufacturing Organization (CDMO) is one of the highest-leverage decisions you’ll make in a biologics...
Why HCP Monitoring Matters in Biologics
Why HCP Monitoring is Critical in Biologics Development Biologics have reshaped modern medicine, providing innovative therapies for cancer, autoimmune conditions, and rare diseases. Their...