Five integrated views — Dashboard, Table, Map, Drug & Devices, and Monitoring — plus Agent-Ready Export for AI agents and data pipelines.
Clinical operations teams waste hours every week toggling between ClinicalTrials.gov, FDA databases, EMA portals, spreadsheets, and internal systems. Trial data lives in silos. Regulatory intelligence is manual. Changes go unnoticed until it's too late.
ClinicaLister consolidates your entire trial portfolio into a single workspace. Follow any clinical trial, and instantly access linked drug approvals, device classifications, patent timelines, adverse event data, canonical disease mappings, and geographic facility intelligence — updated throughout the day from 18+ authoritative sources including the Monarch Disease Ontology (MONDO).
Every view is cross-filtered and connected — work in the way that makes sense for your team.
50+ clickable charts provide instant visual analysis of your trial portfolio. Phase distribution, recruitment status, geographic spread, sponsor concentration, drug sources, device classifications, canonical disease breakdowns, and more — each chart element acts as a cross-filter that refines every other view. A rare-disease toggle instantly narrows the entire portfolio to Orphanet-classified indications.
Key benefit: Identify portfolio trends and gaps in seconds, not hours.
A fully customizable data table with sortable columns, multi-select filters, and user-defined custom columns. Track proprietary attributes like internal priority scores, competitive assessments, or review notes — then export everything to Excel with a single click.
Key benefit: Your trial data, organized exactly the way your team works.
Interactive world map with facility marker clustering, detailed site information on click, and polygon-based geographic filtering. Draw a custom boundary around any region, and every view instantly filters to show only trials within that area.
Key benefit: Understand your geographic exposure and identify site concentration risks at a glance.
The most data-rich view in the platform. Every trial in your portfolio is automatically linked to relevant FDA drug approvals, EMA medicines, and FDA device submissions. AI-identified suggestions are transparently scored and community-validated. Expand any link to access patents, exclusivity periods, biosimilar landscapes, substance data, adverse events, recall histories, and EU trial cross-references.
Key benefit: Regulatory intelligence integrated directly into your trial workflow — no separate system needed.
Automated change detection tracks modifications across your entire portfolio and classifies each change by severity — Critical, High, Medium, or Low. A visual timeline shows when changes occurred, a sponsor activity matrix reveals modification patterns, and an AI assistant explains what changed and why it matters.
Key benefit: Never miss a protocol amendment, status change, or enrollment update again.
ClinicaLister's cross-filtering engine ensures that every action in one view cascades to all others:
Click a phase in the Dashboard chart → Table, Map, Drugs, Devices, and Monitoring all update
Draw a polygon on the Map → Dashboard charts recalculate for that geographic area
Filter by a drug name in the Drug & Devices tab → Dashboard and Table show only trials linked to that drug
Pick a canonical disease (or its entire subtree) → All views narrow to matching trials, deduplicated across every vocabulary variant
Toggle "Rare diseases only" → Every chart, table row, and map marker instantly reflects the Orphanet-flagged subset
Apply a date range in the header → Every view reflects the time window
This eliminates the need to re-filter in each view and ensures your team always sees consistent, contextual data.
Export your entire regulatory intelligence portfolio in a single structured file — ready for AI agents, data pipelines, or team analysis.
Download a single XLSX file containing 22 cross-linked data sheets — trials, drugs, devices, patents, safety data, substances, and more. An embedded AI prompt provides context for automated analysis. Smart chunking handles large portfolios, and all active filters are preserved in the export.
Work from a single source of truth with shared data and intelligence.
Create teams, invite members, and assign roles with granular access controls.
Follow and manage trials as a team, with batch follow/unfollow across the entire portfolio.
Build and share query libraries across your team for consistent trial identification.
Flexible licensing across personal, team, and organization sources — the most permissive license always applies.
Connect AI assistants like Claude directly to your ClinicaLister data through the Model Context Protocol (MCP).
Ask questions about your portfolio in plain language and get answers grounded in your live regulatory data. The MCP integration gives AI assistants direct, secure access to your ClinicaLister workspace — no copy-pasting or manual exports required.