Investigator-initiated trials, from PHRC to publication.
University hospitals, research institutes, learned societies: we support your investigator-initiated trials, long-term registries and cohorts. Pricing adapted to the public sector, methodological support included, HDS hosting for your patient data.
A French CRO that speaks the language of DRCI
More than 20 academic partners trust us — Inserm, Institut Pasteur, Institut Bergonié, CHU de Toulouse, Nantes and Poitiers among our references. A French, agile CRO adapted to the constraints of the public sector.
Investigator-initiated trials (RIPH)
Jardé law compliance (RIPH 1, 2, 3), methodological support for the protocol, CPP/ANSM submissions, pharmacovigilance follow-up. Expertise on PHRC-funded studies.
Long-term registries & cohorts
Platform adapted for multi-year follow-up: CDMS versioning, amendment management, automated quality controls, periodic exports. HDS hosting for the full duration.
Methodological support
Biostatistical advice upstream of the protocol, sample size calculation, endpoint selection, analysis plan. Support for drafting the statistical section of your dossier.
Publication support
Clean CDISC datasets, SAS analyses, tables and figures to major journal standards. Support for drafting the results section and reporting negative results.
An academic study to structure?
Investigator-initiated trial, PHRC response, patient registry or cohort — describe your project and we will respond with a methodological framework adapted to the public sector within 24 business hours.
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