04/05/2026
Clinical data integration is no longer a matter of efficiency. It's a matter of operational integrity.
The complexity of modern clinical research, accelerated by AI and an expanding regulatory perimeter, has exposed the cost of fragmented systems. Disconnected data is no longer a tolerable trade-off.
Synvia TrialCore was engineered to address this directly: an integrated digital ecosystem that consolidates eCRF, CTMS, ePRO, and eTMF within a single environment. Sponsors, CROs, and investigators operate over the same source of truth, eliminating reconciliations and parallel workflows.
Built inside Synvia, the largest clinical research operation in Latin America, TrialCore was designed with FDA, 21 CFR Part 11, EMA GCP/GLP, ANVISA, ICH, and LGPD compliance embedded in its architecture, not retrofitted.
Interested in how we are rethinking the infrastructure of clinical trials?
Join us at the 16th Annual Outsourcing in Clinical Trials Europe 2026, in Barcelona, this Wednesday and Thursday — Booth 47.
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