EURAXI provides either a global or an à la carte service offering in taking on your clinical trial projects: interventional or non-interventional and in different pathologies and fields of expertise.

Our proven, multidisciplinary and reactive team will guide you on your projects, every step of the way.

Interventional studies

– From writing the synopsis to publishing your interventional study projects
– Euraxi provides sound advice on choosing the right methodology
– We conduct feasibility studies
– We select sites within France or Europe
– We prepare documents required for regulatory submissions
– We follow up your projects as per GCP
– We manage investigational products (dispatching of treatments, etc.)

Observational studies

– From writing the synopsis to publishing your observational study projects: observatory, registry, case-control, PASS (Post-Authorisation Safety Study), PAES (Post-Authorisation Efficacy Study), etc.
– For all your studies in town (at the doctor’s surgery), at the hospital or at a pharmacy
– We take care of site selection and initiation
– We design and follow up the production of kits containing study materials and equipment
– We create dynamic dashboards accessed via a project-specific website (downloads, graphic standards, profile-managed access rights, dynamic maps)


– We offer an experienced team of CRAs operating throughout France
– We conduct on-site or remote monitoring visits
– We handle all types of visit from site selection through to close-out
– We carry out quality control visits and audit preparation

Investigator support

– We provide you with a regional team of clinical research technicians and study nurses
– Our offer includes data entry and query management via paper CRF or eCRF
– Our study nurses provide paramedical services including vital sign recording, ECGs, ABPMs (etc.), biological sampling, centrifugation, labelling, etc.
– We assist practitioners with patient screening
– We organise study logistics

Support vigilances

Our team of vigilance experts assists you in:
Managing cases and writing up oral statements
– Establishing automatic e-mail alerts
– Conducting quality controls
Writing up safety reports