Simplified access to our specialized health data warehouses. Multi-project studies possible in 3 to 6 months thanks to simplified reference methodologies.
Our EDS cover all medical specialties with large patient populations and robust longitudinal histories.
Specialized cardiology database. SFC registries, comprehensive data on cardiovascular diseases.
Urological oncology. AFU registry specialized in kidney cancer and prostate cancer.
Pulmonology and COPD database. SPLF data for respiratory diseases.
Gynecology-obstetrics database from CHU Bordeaux. 134 participating centers, obstetric and gynecological data.
Representative primary care data. 3,050 general practitioners, 15 years of history.
Community pharmacy database. 85% of French pharmacies, longitudinal medication data.
Pharmacoepidemiological and health-economic studies conducted on our data warehouses linked to SNDS.
Analysis of the incidence, predictive factors and long-term outcomes of reinterventions (TAVI explantation, redo TAVI) after initial transcatheter aortic valve implantation, from the France TAVI registry of the SFC linked to SNDS.
Observational study on the VIGIMESH+ registry linked to SNDS. Quantification of reintervention rates for complication or recurrence of stress urinary incontinence at 1, 2 and 3 years after SUS implantation in 3,671 patients between 2017 and 2020. HAS/CNEDIMTS opinion issued.
Assessment of the time between idiopathic pulmonary fibrosis (IPF) diagnosis and death, comparing early (<3 months) vs late (≥3 months) initiation of antifibrotic treatment. Study conducted on the Colibri-PID cohort linked to SNDS, under the responsibility of BI and Clinityx.
Longitudinal study on kidney cancer from the national UroCCR database (AFU, CHU de Bordeaux) linked to SNDS. Analysis of therapeutic strategies, overall and progression-free survival, and assessment of the complete care pathway over 14,300+ patients from 41 centers. CNIL authorization for 10 years.
Find all our research projects on Semaphore, our transparency portal.
Pre-validated procedures that accelerate your data access.
No CESREES application required. Pre-authorized methodologies from the CNIL accelerate authorizations.
Deploy multiple studies in the same EDS without restarting procedures. Timeline reduced at each iteration.
3 to 6 months from protocol to data delivery. Our EDS are stable and well-documented.
Linkages are completed and cross-referenced EDS-SNDS data is immediately available. No additional delay to access linked data.
From research question to publication, a simplified process thanks to pre-authorized reference methodologies.
Selection of the appropriate EDS and validation of the research question.
1-2 wks
Protocol writing and simplified declaration (no CESREES required).
3-4 wks
Protocol validation by the scientific committee of the partner EDS.
2-4 wks
Data extraction and analysis in a secure environment according to the validated protocol.
6-10 wks
Final report and support for scientific submission.
3-4 wks
For your next study, simply access our data warehouses with simplified reference methodologies.