In the Product
Real answers, from a demonstration trial.
Ask Vivo answers questions about your trial data, contextualized by the study's own documents. Every answer ships with human-reviewable reasoning steps and the query that produced it — and agents run under the user's own permissions.
Ask Vivo gives clinical development teams a governed AI interface to their own trial data, documents, protocol context, and operating workflows.
"Ask the trial. See the evidence."
Each agent queries the governed data model, applies domain reasoning, and surfaces prioritized findings with the evidence attached. Agents inherit the user's permissions — one instance per role, blinding-aware by design.
Site 8 has 32 screen failures — top causes identified from screening logs. Recommendation: CRA review at Site 8; redistribute recruitment to two lower-failure sites with capacity.
Cross-references ICH E2A reporting obligations: flags SAEs missing narratives or causality assessment while reporting windows are still open — before they become findings.
Site 3 far exceeds the trial mean for discrepancies; two sites identified as best-practice models. Reusable rules proposed for the recurring patterns.
Surfaces trends and hypotheses on endpoints and subpopulations — divergences by baseline strata, deviation-driven population gaps — each with the analysis attached for review.
Plus the plot agent: data visualizations and analyses generated on demand, with the code attached.
Every answer is scoped to the asker's role and blinding status, enforced at the data layer — arm-level views require unblinded permissions.
"Vivo is our new best friend."
Medical Monitor · Phase 2 Rare Disease TrialGoverned, auditable, role-aware AI over your live trial data — in production with sponsors today.