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GTP Bioways Facilities

GTP Bioways operates 4 facilities, specialised in process development and cGMP manufacturing of biotherapeutics, nanodrugs and bioconjugates.

 

GTP Bioways has the financial support of Occitanie region.

 

 

Labège (France): our process development facility – a seasoned team devoted to your projects

The facility is dedicated to R&D production and process development activities, with R&D & pilot rooms for microbial fermentation, cell culture and purification activities and a fully equipped analytical lab

Our process development team is composed of seasoned and highly qualified professionals that have collectively managed the production of over 800 different proteins.

Cell line Development process

Toulouse (France): our mammalian and microbial GMP manufacturing suites, together with CLD and aseptic filling capabilities

In Toulouse, our teams’ expertise covers fill and finish for a wide range of active pharmaceutical ingredients as well as the formulation, process development and GMP manufacturing of nanodrugs. Our GMP suites for mammalian and microbial manufacturing and our Cell Line Development laboratories are also located in this facility.

The facility comprises 500 sqm of laboratory including 50 sqm of clean rooms (ISO 8 and 7, and ISO 5 under isolator) for drug product manufacturing and 400 sqm for GMP suites for drug substance manufacturing.

Our team is composed of seasoned scientific experts and managers with over 20 years’ experience in sterile manufacturing.

Saint-Julien-en-Genevois (France): our cGMP manufacturing facility for mAbs and ADCs

Our St-Julien team’s expertise encompasses the manufacturing of biologics and antibody-drug conjugates.

This facility is located in Saint-Julien-en-Genevois, France and is only a few kilometres away from the swiss boarder and Geneve.

This cutting-edge GMP production unit is equipped with the most recent single-use technologies to offer flexible manufacturing capacities and short turnaround times.

Thanks to our expert technical team with over 15 years’ experience and our seasoned QA experts, we have  successfully brought a variety of antibodies and antibody-drugs conjugates to the clinic.

Veyre-Monton (France): immuno-assays and HCP risk management experts

Our team is specialised in immunoassays development and implementation of quality and safety controls of raw and processed biological materials.

With our seasoned team, we are able to develop process-specific HCP ELISA kits from scratch as well as tailor-made immunoassays for a wide range of applications (target bioprotein quantification, potency assays, …).

This facility is located in Clermont-Ferrand area, France. All the activities performed are covered with ISO 9001v2015 certification.

GTP Bioways CDMO - Bioconjugates Analytical Development

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A Guide to Smooth CDMO Tech Transfer

The key parameters to be considered while choosing your next CDMO, as well as our tips to assess those parameters, and more!

Discover more about GTP Bioways services

Biologics

Bioconjugates

Nanodrugs