GMP production services
Our GMP-licensed facility is purpose-built for early-phase clinical trials – designed for fast-moving timelines, small batches, on-site production, adaptive protocols and close coordination with clinical floor staff. Everything is handled on-site, within meters of our clinical beds, enabling small-scale, high-flexibility production with minimal stability data and full clinical supply support.
We offer Non-sterile manufacturing of IMPs, such as capsules and solutions for internal use Primary and secondary packaging, including trial-specific labeling EU import, batch certification and QP release of IMPs produced outside Europe – including aseptically prepared sterile products and biologicals (e.g. challenge agents, immunologicals) Distribution to clinical sites in Belgium and across Europe in full compliance with good distribution practice (GDP) standards
Our production facility holds GMP license 1289 IMP and meets all GDP requirements for distribution. Want sterile capabilities? Our brand-new Class B cleanroom is ready and currently undergoing accreditation – this service will be added soon.
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