Trusted by leading life science organizations and partners
Accelerate Timelines | Reduce Risk | Improve Outcomes
Trusted by leading life science organizations and partners
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.
Where data lives today
For clinical teams managing active trials, Vivo becomes the operating layer above EDC, CTMS, labs, safety, imaging, IRT, and documents.
Bring clinical, operational, safety, quality, document, and specialty data into one governed layer. Full source traceability preserved.
Ask questions in plain language. Receive source-backed answers grounded in live trial data, protocol context, and evidence — not guesses.
A continuously updated operating surface: what's the trial status? What changed? What needs attention? What actions are pending?
AI-RBQM continuously watches for missing, late, inconsistent, or high-risk patterns. Signals become alerts → issues → evidence packages.
Cross-study visibility into risks, sites, vendors, enrollment, data quality, and executive priorities — from one trial to an entire portfolio.
HIPAA, GDPR, GxP, Part 11/Annex 11, SOC 2, ISO 27001, ISO42001, ISO 9001. Source traceability, RBAC, blinding-aware, audit trails.
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.
"Ask Vivo allows me to get real time answers to all the questions I had spent weeks answering in Excel."
Safety Monitor · Global Phase 2 CNS TrialVivo gives each team the visibility, evidence, and workflow they need — while keeping everyone aligned around the same source-backed operating picture.
Run active trials with earlier visibility and fewer manual reports. Track status, enrollment, sites, vendors, and issues.
Explore →Find data issues earlier. Prove readiness with traceable evidence. Discrepancy → query → sign-off → lock readiness.
Explore →Review safety signals in clinical context. Connect AEs, labs, conmeds, dose, and subject patterns with source-backed evidence.
Explore →Know which studies, sites, vendors, and programs need attention. See cross-study risk before issues escalate.
Explore →Power internal copilots, analytics workbenches, and agent ecosystems with governed, protocol-aware clinical trial intelligence.
Explore →Give sponsors more transparency with less manual reporting. A shared evidence layer for delivery accountability and quality oversight.
Explore →Start with your most pressing operational challenge. Vivo delivers value on day one and expands across your workflows.
Replace delayed reports and spreadsheets with a live view of what changed and what action should follow.
Detect discrepancies, monitor completeness, track review state, and prove readiness with traceable evidence.
Understand enrollment progress, screen failure drivers, site performance, and retention risks earlier.
Investigate signals with subject-level context and source-backed evidence across AEs, labs, conmeds, and dose.
Give clinical development leaders a shared operating picture across studies, sites, vendors, and programs.
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."
VP, Clinical Operations · CNS-Focused Biotech · Global Phase 2 Alzheimer's TrialEDC · CTMS · Labs · Safety · Imaging · eCOA · IRT · Wearables · TMF · Vendor Files
Harmonized · Governed · Traceable · AI-ready · Role-aware
Protocol-aware · Source-backed · Explainable · Role-aware
Alerts · Issues · Evidence Packages · Risk Signals
Trial Home · Ask Vivo · Workflows · APIs · Portfolio Views
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."
Vivo is designed for governed AI use, with source-backed answers, role-aware permissions, audit trails, human review, and study integrity safeguards.
"Trust does not come from confidence. Trust comes from traceability."
Vivo helps teams move from fragmented trial data to governed, source-backed oversight without waiting quarters for value.
"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.
NVIDIA Inception Program
Johnson & Johnson JLABS
DCRI Program Finalist
PharmStars - R&D Accelerator Finalist
DayOne - Top 3 Innovator
DPHARM Idol Competition Finalist
LabConnect Partner, LIMS Integration
Innovation Network The Gathering - Top Innovator Award
Medidata - Member, Developer Central
See how Vivo helps clinical development teams unify live trial data, ask source-backed questions, detect risk earlier, and turn insight into governed action.