We design studies that match your strategic goals and timelines, optimizing the data to be collected, with input from HCPs and patients.

We oversee the full clinical study lifecycle, from strategy to operations, delivering high-quality evidence efficiently and in compliance with regulations.

We organize and manage site selection, initation visit, monitoring visits and perform close-out visits.

We submit your studies to the ethics committee and regulatory authority, and ensure continues communication throughout your study

We connect innovators with patients to capture real-world insights, ensuring studies, products, and services meet the needs of those living with life-impacting conditions.

We build strong partnerships with investigators, KOLs, and study committees to bring expert insight and collaboration into every phase of your clinical research.

We set up and manage steering committees, advisory boards, and data review groups to provide your study with strong clinical guidance and effective oversight.

We organize and manage your investigator and study coordinator meetings, remote or on location.

Currently we provide services directly in Belgium, The Netherlands and France.

We cover the rest of EU and USA through partners.