4.2M+
trial and outcome records indexed
Normalized across registries and filings with daily refreshes and full provenance on every datapoint.
< 3 min
median time to first credibility snapshot
Purpose-built flows for diligence sprints, IC prep, and reactive readouts without leaving the workspace.
99.95%
quarterly API availability (internal SRE)
Enterprise controls including SSO, scoped API keys, and region-aware hosting for regulated workflows.
Evidence fabric
Trial arms, endpoints, amendments, and safety tables are harmonized with regulatory correspondence and selected literature so analysts see one timeline per asset, not twelve tabs.
- Registry + FDA / EMA metadata with automated change detection
- Curated PubMed and congress layers with conflict resolution
- Document vault for LOIs, briefing books, and IC packets
Scoring engine
Methodologies combine statistical design, endpoint rigor, patient granularity, and regulatory fit into a transparent score with drill-down to underlying drivers. Versioning lets you replay decisions against past model generations for governance.
Scores export to CSV, PDF briefs, or your data warehouse through scheduled jobs or on-demand pulls.
Alerts and watchlists
Standing watchlists merge program tags, therapeutic areas, and portfolio holdings. Alerts fire on new outcomes, label changes, safety signals, or competitor milestones—routed to Slack, email, or webhook endpoints your team already uses.