We offer a comprehensive suite of services for clinical trials and medical device/IVD projects. These include, but are not limited to: regulatory affairs, biostatistics, project management, document & trial master file management, clinical operations, clinical data management, medical & scientific writing, product vigilance, legal representation, and sponsorship as a service.

No. We operate globally. Through our own offices and international partners, we can support trials both inside and outside Europe.

We can work in full-service mode, managing all aspects of your trial or medical device project, or in a functional service provider model, where you select only the services you need.

Yes. We support regulatory affairs roles for medical device and IVD projects, which includes preparing documentation such as Clinical Evaluation Reports (CERs) including accompanying literature search, Post-Market Clinical Follow-Up (PMCF) reports, and technical documentation.