The running trial, and the data behind it, in one view.

Vivo is the control tower for your active trial: what's happening, what changed since you last looked, what needs your attention, and the recommended action — always in view, always traceable to source.

Trial Home — Daily View

Trial status: On track. 3 items need attention.
Site 104: Enrollment 40% behind plan — 18 days no screenings
Safety signal: AE cluster at Site 104 (Cohort B) — review recommended
Central lab feed: data refresh overdue by 3 days
12 other items unchanged since last review
Last updated: 4 hours ago · Next refresh in 2h
Trial Home

Know what changed before the meeting starts.

Trial Home gives study teams a continuously updated view of what is happening across the trial, what changed since the last review, what needs attention, and what actions are pending. Designed for the rhythm of real clinical development work.

  • Current status across enrollment, sites, vendors, data quality, safety, and protocol
  • What changed since the last review cycle
  • Emerging risks that require attention
  • Open alerts, issues, assignments, and review items
  • Trial News summaries for cross-functional teams
Study Operations & Safety Oversight

Oversee active trials and the data behind them.

Every oversight view drills through to the underlying records — subject, visit, site, and source — so review never ends at a chart.

Enrollment tracking & forecasting

Actual vs. planned screening and enrollment, with trial- and site-level forecasts — slippage visible while there is still time to act on it.

Participant profiles & timelines

The full subject picture — history, events, visits, and measures on one longitudinal timeline.

Safety oversight & DSMB prep

AE and SAE review in clinical context, with evidence packages assembled for DSMB and safety committees.

Every measure, inspectable

Labs, questionnaires, assessments, and ECG intervals over time — plus imaging reads with read operations, turnaround, and e-signature status where imaging vendors are connected.

Comparative site performance

Enrollment, deviations, data quality, and visit compliance ranked across sites — best practices surfaced, laggards flagged.

Insights, alerts & actions

Scheduled analyses run on your cadence. Findings arrive as alerts, and alerts become tracked actions with owners and history.

Every one of these views is a workspace: filter it, plot it, save it, export it — the same pattern on every dataset in the trial, from adverse events to imaging reads.

In the Product

The running trial, in the product.

Individual subject profile in Vivo: longitudinal timeline of dosing, safety events, and measures with an event details panel
One participant, whole story — dosing, safety, and measures on a single timeline. Demonstration trial, synthetic data.
Vivo safety overview: adverse event KPIs with incidence and causality rankings
Safety oversight at a glance — the evidence a DSMB prep starts from. Demonstration trial, synthetic data.
Trial Site Oversight

Site startup, conduct, and closeout — tracked end to end.

Vivo tracks each site's lifecycle via ISF and TMF integration: activation progress, document readiness, conduct signals, and closeout status — connected to the same operating picture as enrollment, safety, and data quality.

  • Startup: activation milestones and document completeness by site
  • Conduct: visit compliance, deviations, and data quality per site
  • Closeout: outstanding queries, reconciliation, and archive readiness

Site Lifecycle

Site 112 · Activated Docs 100%
Site 118 · In startup 2 docs pending · 12 days to target
Site 097 · Closeout 4 open queries
ISF & TMF integrated · document status straight from the source systems

"Our CMO went from spending a week plus manually collating and creating the various tables he wanted for DSMB to maybe 30, 45 minutes. That's just transformative to how we do business."

VP, Clinical Operations · Alzheimer's Disease Global Phase 2 Trial

Stop assembling status. Start acting on it.

Live with sponsors today. Most teams are running active trial oversight in 6–8 weeks.