Based on three decades of experience on databases dedicated to clinical trials, we have created a modular solution fitted to your needs.
Coding tool
IVRS modules/ IWRS modules
Module for managing the investigational products
Complete and flexible CDM solution (Clinical Trials Module)
customable eTMF (DIA model or your model)
eCRF, pCRF
ePRO
Connector to API external sources
Uploading of medical imaging or photographs after pseudonimization
Co-founded in 1998 by RCTs, ClinInfo is a Lyon-based company specializing in eClinical solutions. Its digital solutions are validated according to industry standards (21 CRF part 11, Gamp5, EU GMP Annex 11, ISO14155: 2012) for any type of study and are suitable for all interventional or non-interventional studies.
Designed according to a “Privacy by design and default” approach in order to guarantee maximum protection of personal data throughout your studies, the ClinInfo solution is deployed in an ISO-27001 certified host approved for hosting health data
Reliable
Highly configurable
Easy to implement
Adaptable to the context of each project
RCTs is a member of the CDISC community and has strong expertise in the design of CRFs in CDASH format and the database locks in SDTM format.
Pre-Authorization Studies
Post-authorization studies on primary data
Secondary Data Studies
Health economics
Clinical Evaluation of MDs / Regulatory consulting
Early / Compassionate Use