We manage your biopharmaceutical manufacturing project as ours
We are committed to ensuring a smooth CMC journey for the development of your biotherapeutics.
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.
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.