Vivo powers internal copilots, analytics workbenches, and agent ecosystems with governed, protocol-aware clinical trial intelligence. Vivo does not replace your internal AI strategy. It accelerates it.
Large pharma organizations are investing in internal copilots, data platforms, analytics workbenches, and agent ecosystems. Clinical trial intelligence requires more than a generic AI interface — it requires live trial data, protocol context, role-aware access, source traceability, evidence generation, evaluation, auditability, and study integrity controls.
"The most interesting thing to us is the Ask Vivo. Could we have a solution like this focused on our own data warehouse?"
Plain-language clinical trial Q&A behind your internal copilots with source-backed, role-aware answers.
Protocol, amendment, visit schedule, endpoints, and safety context built into every reasoning call.
Sponsor-defined risk rules, thresholds, and protocol events monitored continuously — outputs via API.
Source records, protocol context, provenance, RBAC, and audit metadata bundled with every output.
Select one active study. Identify priority data sources and use cases. Establish governance and access. Define success metrics and configure initial Ask Vivo question set.
Load and harmonize priority data. Configure role-aware Ask Vivo workflows. Demonstrate source-backed answers. Pilot recurring insights or alerts for priority risks.
Measure answer quality, usefulness, adoption, and operational value. Define integration paths. Identify additional studies and use cases. Produce enterprise deployment recommendation.
Vivo gives large pharma teams a governed clinical trial intelligence layer that can power internal copilots, data platforms, analytics workbenches, and agent ecosystems.