Our experts

Our team brings together expertise in pharmacy, GMP manufacturing, quality assurance, regulatory affairs, and the development of cell and gene therapies. We combine hands-on experience in cleanroom production with deep knowledge of the rules and standards that apply to medicines for clinical trials. Working closely together, we guide each project from development through manufacturing to the release of the finished product.

We are committed to reliable, high-quality work and to supporting researchers, clinicians, and other partners every step of the way.

Two persons working in the QC laboratory

Person sitting behind microscope and looking through oculars in cleanroom

About our team

Our team combines a broad range of expertise needed to bring cell and gene therapies and challenge agents safely from the laboratory to the patient. Together we cover pharmacy, GMP manufacturing, quality assurance, quality control, regulatory affairs, and process development. This means that within one team we can develop a manufacturing process, produce a product under GMP conditions, test it, and prepare it for use in clinical trials.

Many of our team members have years of experience in their field, and we work in close collaboration so that knowledge is shared across disciplines. We collaborate with research groups within the hospital, and with academic and other partner groups both nationally and internationally (e.g. DARE-NL, ReNEW, MuSICC, CORE-ATMP, IMPACT, P-SMART). Because cell and gene therapy is a fast-moving field, we invest continuously in training and education. Team members are trained for their specific tasks and regularly update their knowledge and skills, so that we maintain high-quality, up-to-date services.

Our team