Unobio

Type in a drug name and find all direct and indirect competitors instantly! Agentic Biopharma commercial intelligence. Minutes of research instead of weeks. One click, one single pane of glass for all your pharma intelligence data.

Generate structured first drafts faster by unifying intake, synopsis inputs, schedule of events, and protocol drafting in a single workflow. Regulatory Intelligence is built for regulatory teams that want a guided process with AI support available when needed—and full control over final content.

Unobio Clinical Trial Search provides a trial-centered workflow for assessing feasibility and risk in a defined clinical domain. Trial retrieval is filterable across common design and execution parameters (phase, endpoints, population characteristics, geography, sponsor activity), enabling comparison of study patterns and operational constraints within an indication. A primary output is a structured risk report that organizes risk factors into scientific/clinical, operational/execution, and competitive domains. The report presents the rationale for each risk item and includes qualitative scoring (likelihood/impact) to support consistent cross-program review. The intent is to reduce time spent on manual aggregation while improving traceability from conclusions back to underlying trial evidence.

Not ready for a massive QMS rollout? Vault is a lightweight eQMS for teams that want compliant workflows now — and flexibility later.

Write clinical protocols faster. Custom schedule of event builder, AI integration, reference creator, and much more fine grained control to speed up the regulatory writing process.

Close CAPAs and change controls faster with an eQMS built for lean teams. Part 11 e-signatures + audit trails + governed workflows. Get a live demo + see an inspection-ready evidence pack