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We manage your biopharmaceutical manufacturing project as ours

We are committed to ensuring a smooth CMC journey for the development of your biotherapeutics. 

GTP Bioways CDMO - CMC Development

A team dedicated to your CMC development

Relying on 25 years of experience as a service provider, GTP Bioways CDMO provides unique support to its clients, from initial request to project close-out.

 

MSc or PhD

All of our project managers have a robust scientific background with a specialisation in biotechnology.

270 clients worldwide

We regularly collaborate with both small biopharmaceutical companies and large pharmaceutical firms.

1,700+ projects

Through over 1,700 CMC development projects, we have navigated significant complexity and encountered a diverse range of biomolecules.

We are committed to designing the best approach to meet your requirements

We believe that understanding your project’s intricacies and constraints is essential to start off with the best strategy and avoid any pitfalls that could delay the programme. To that effect, we have a team of scientific experts dedicated to crafting our proposals.

Using our strong scientific knowledge and industry experience, we will advise on the most relevant technical approach to meet the specific challenges of your project and collaborate with you to design a scope of work that aligns with your technical requirements, while keeping in mind your timelines and budget constraints.

Cell line Development process
Cell line Development process

Benefit from our CDMO expertise throughout your bio manufacturing project

Throughout the project, you will benefit from the support of a highly-skilled project manager, who will be your main point of contact. The  Project Manager’s role is to plan and coordinate the completion of development and manufacturing activities, ensuring the agreed objectives are met and keeping track of the project status through clear and timely communication.

We deem it crucial for our clients to have direct access to our technical experts (Process Development, Analytical Development, Quality Control, Quality Assurance, and GMP Manufacturing) for the efficient management of project intricacies.

When the project closes, we  organise wrap-up discussions, to gather client feedback and identify areas of improvement. Where there is a technology transfer, we will continue providing the necessary support until successful transfer to the receiving unit.

Our highly-skilled scientists guide you through the development of your biopharmaceuticals

GTP Bioways CDMO

Our vision & values

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Full-service CDMO

GTP Bioways CDMO

Science-driven CDMO