The Control Tower for
Clinical Development
Accelerate Timelines | Reduce Risk | Improve Outcomes
Clinical trials move faster than the systems used to manage them.
Trial data is scattered across vendor portals, CRO reports, spreadsheets, EDC, CTMS, labs, safety systems, imaging, eCOA, IRT, documents, and specialty data sources. Study teams still assemble status manually, reconcile updates after the fact, and wait for periodic reports to understand what changed.
Risk doesn't wait for the next report.
Enrollment delays, safety patterns, protocol deviations, vendor issues, missing data, and endpoint risks often become visible only when data is connected across systems. Vivo creates the missing operating layer.
Connect, Ask, Monitor, Act.
For clinical teams managing active trials, Vivo becomes the operating layer above EDC, CTMS, labs, safety, imaging, IRT, and documents.
Unified Trial Data
Bring clinical, operational, safety, quality, document, and specialty data into one governed layer. Full source traceability preserved.
Ask Vivo
Ask questions in plain language. Receive source-backed answers grounded in live trial data, protocol context, and evidence — not guesses.
Trial Home
A continuously updated operating surface: what's the trial status? What changed? What needs attention? What actions are pending?
Continuous Monitoring
AI-RBQM continuously watches for missing, late, inconsistent, or high-risk patterns. Signals become alerts → issues → evidence packages.
Portfolio Intelligence
Cross-study visibility into risks, sites, vendors, enrollment, data quality, and executive priorities — from one trial to an entire portfolio.
Governed & Validated
HIPAA, GDPR, GxP, Part 11/Annex 11, ISO 27001, ISO 9001. Source traceability, RBAC, blinding-aware, audit trails.
Source-backed answers to the questions clinical teams actually ask.
Ask questions about live trial data, protocol context, site performance, safety patterns, enrollment status, and data quality — and receive answers that trace back to the underlying evidence.
Plain-language questions over live trial data and documents
Answers grounded in source records with evidence links
Protocol and amendment context built in
Role-aware — you see what's appropriate for your function
Governed, auditable, not a standalone chatbot
Which sites are underperforming against enrollment expectations this week?
3 sites are currently below plan by >20%: Site 104 (Netherlands, 40% behind), Site 211 (Canada, 28% behind), Site 308 (Germany, 22% behind). Site 104 has had 0 new screenings in 18 days. Site 211 shows elevated screen failure rates tied to inclusion criterion IE-03.
Are any adverse events clustered by site, cohort, or dose in the past 4 weeks?
Yes — injection-site reactions are 3.2× higher at Site 104 vs. study mean. All 7 cases are in Cohort B (high dose). No similar clustering in Cohorts A or C.
"Ask Vivo allows me to get real time answers to all the questions I had spent weeks answering in Excel."
Built for cross-functional clinical development teams.
Vivo gives each team the visibility, evidence, and workflow they need — while keeping everyone aligned around the same source-backed operating picture.
Clinical Operations
Run active trials with earlier visibility and fewer manual reports. Track status, enrollment, sites, vendors, and issues.
Data Management & Biometrics
Find data issues earlier. Prove readiness with traceable evidence. Discrepancy → query → sign-off → lock readiness.
Safety & Medical Monitoring
Review safety signals in clinical context. Connect AEs, labs, conmeds, dose, and subject patterns with source-backed evidence.
Portfolio Leadership
Know which studies, sites, vendors, and programs need attention. See cross-study risk before issues escalate.
Enterprise AI & Innovation
Power internal copilots, analytics workbenches, and agent ecosystems with governed, protocol-aware clinical trial intelligence.
CRO & FSP Partners
Give sponsors more transparency with less manual reporting. A shared evidence layer for delivery accountability and quality oversight.
Where clinical teams use Vivo first.
Start with your most pressing operational challenge. Vivo delivers value on day one and expands across your workflows.
Trial Oversight
Replace delayed reports and spreadsheets with a live view of what changed and what action should follow.
Data Quality & Readiness
Detect discrepancies, monitor completeness, track review state, and prove readiness with traceable evidence.
Enrollment & Retention
Understand enrollment progress, screen failure drivers, site performance, and retention risks earlier.
Safety Review
Investigate signals with subject-level context and source-backed evidence across AEs, labs, conmeds, and dose.
Portfolio Intelligence
Give clinical development leaders a shared operating picture across studies, sites, vendors, and programs.
Real-Time Trial Readiness
Prepare for continuous oversight models with unified data, monitored signals, human review, and evidence packages.
"A global trial of this size is vast, and Vivo will be critical in our ability to analyze cognitive results. We can amplify our clinical teams' capabilities, turning complex data into actionable insights at unprecedented speed — which means we can get answers, and treatments, to patients faster."
Data Sources
EDC · CTMS · Labs · Safety · Imaging · eCOA · IRT · Wearables · TMF · Vendor Files
Unified Clinical Trial Data Layer
Harmonized · Governed · Traceable · AI-ready · Role-aware
Agentic Reasoning Layer
Protocol-aware · Source-backed · Explainable · Role-aware
Monitoring & Evidence Layer
Alerts · Issues · Evidence Packages · Risk Signals
Action Layer
Trial Home · Ask Vivo · Workflows · APIs · Portfolio Views
Clinical-grade AI, purpose-built for modern clinical trials.
Not a static dashboard. Not a standalone chatbot. Vivo is the intelligence and action layer above your clinical trial systems of record — a five-layer architecture that unifies data, reasons over trial context, monitors for risk, and supports governed action.
"The hard part is not answering one question. The hard part is answering the right question from the right data, for the right user, with the right evidence, at the right time."
See the Full Architecture →Clinical AI must be explainable, permission-aware, and reviewable.
Vivo is designed for governed AI use, with source-backed answers, role-aware permissions, audit trails, human review, and study integrity safeguards.
Explore Trust & Validation →"Trust does not come from confidence. Trust comes from traceability."
From plan to live insight in weeks.
Vivo helps teams move from fragmented trial data to governed, source-backed oversight without waiting quarters for value.
Plan
Select trial, users, data sources, use cases, governance, and success criteria.
Connect
Integrate priority clinical, operational, safety, quality, and vendor data sources.
Configure
Activate Trial Home, Ask Vivo, dashboards, alerts, issues, and role-based access.
Launch
Train users, monitor adoption, refine workflows, begin active trial oversight.
Scale
Extend across additional studies, portfolios, functions, and enterprise AI ecosystems.
"Clinical trials are drowning in complexity and data silos. With Vivo, we've built the first agentic AI control tower to unify data and deliver real-time, explainable insights. Our goal is simple: help trial teams act faster, reduce costs, and bring life-changing treatments to patients sooner."
We are on a mission to transform clinical trial operations to deliver life-changing medicines to patients faster.
Latest News
Stop waiting for trial status updates.
See how Vivo helps clinical development teams unify live trial data, ask source-backed questions, detect risk earlier, and turn insight into governed action.
