Track 590,300+ trials across 18+ databases — unified by a substance-level knowledge graph, not a list of sources. Get instant alerts. Stay ahead.
Dramatically reduce manual research time with automated competitive intelligence that connects clinical trials to 18+ databases including FDA drugs, EMA medicines, devices, patents, and the MONDO disease ontology — plus a canonical disease layer that unifies every synonym and subtype, with instant alerts when competitors change strategy.
Stop wasting hours every week on manual research across 18+ databases. Automated 24/7 monitoring delivers critical competitor changes to your inbox — patent cliffs, trial terminations, biosimilar approvals — before your competition even knows they happened.
Hours of weekly manual research. Missed opportunities. Competitive blindspots.
Your team is drowning in manual research while competitors act on automated intelligence.
Every competitive intelligence report means toggling between ClinicalTrials.gov, FDA Drugs@FDA, EMA databases, GUDID, patent databases, and more — manually copy-pasting data across disconnected systems.
Impact: Manual work that should be automated — freeing your team for strategic analysis
When competitors terminate trials, change sponsors, or shift geography — every hour of delay in discovering these moves costs market advantage. Manual checking means you find out days or weeks too late.
Impact: Competitors adjust their strategy based on real-time intelligence while you're still gathering data
Evaluating a major partnership or planning market entry without seeing patent timelines, biosimilar landscapes, and regulatory approval status alongside trial data? That's gambling with incomplete intelligence.
Impact: One missed patent expiration or biosimilar approval could invalidate your entire market entry strategy
By the time you manually discover that a competitor terminated a trial, shifted enrollment, or added new sites — they've already adjusted their strategy and moved ahead.
Impact: Manual monitoring means you're always reacting to yesterday's news while competitors act on today's intelligence
While your team manually searches 18+ databases for hours each week, competitors with automated intelligence are already acting on the insights you haven't even discovered yet.
Wasted on manual research, database switching, and data copy-pasting that should be automated
Manually searched and cross-referenced — time that could fund strategic initiatives instead
Finding out about critical competitor moves — giving rivals a head start on strategic response
Every day you delay automating competitive intelligence, you're falling further behind.
Patent expirations. Trial terminations. Biosimilar approvals. Enrollment changes. Geographic shifts. Competitors are acting on these signals in real-time while you're still manually searching.
Never Miss a Competitor Move. Make Faster, Smarter Decisions.
Automated competitive intelligence that connects 590,300+ trials with FDA and EMA data — delivering the insights you need in seconds, not hours. While competitors manually search, you act.
Stop wasting time toggling between 18+ databases. One search replaces hours of manual cross-referencing. Automated alerts replace daily checking. Get your time back.
Get instant alerts when trials change status, sponsors, or locations. See exactly what changed with before/after diffs. Act on intelligence while competitors are still searching manually.
See the full picture in seconds: trial data + FDA approvals + patent timelines + biosimilar landscapes + device recalls. No guessing. No incomplete intelligence. Just complete context.
While competitors manually search for hours and discover changes weeks late, Clinicalister users act on automated intelligence the same day it happens.That's the competitive advantage of real-time intelligence.
Eliminate hours of weekly manual research
Know when competitors move before your competition does
Full regulatory context for strategic decisions
Before: 2+ hours daily manually checking 18+ databases for competitor changes.
After: 5-minute daily digest with automated alerts delivered to your inbox.
Reclaim your research time with 44 interactive charts, automated monitoring, and complete FDA/EMA regulatory intelligence in one unified platform.
Saved on manual database checking
Changes surface within hours, refreshed throughout the day
Automated monitoring while you sleep
This automated dashboard replaces 2+ hours of daily manual work with a 5-minute digest delivered to your inbox.
44 interactive charts • 5 integrated views • Complete FDA/EMA regulatory intelligence • Real-time automated alerts
❌ Manual Process:
✓ ClinicaLister:
While competitors spend hours weekly manually researching across 18+ databases, you're getting automated intelligence delivered to your inbox.That's the competitive advantage of automation.
Stop switching between databases for trial research. One search across 590,300+ trials with FDA/EMA data replaces manual database hopping. Pick a canonical disease from the MONDO ontology and automatically match every synonym, alias, or subtype.
Replace hours of spreadsheet analysis with instant visual intelligence. See market dynamics, competitor activity, and strategic opportunities at a glance.
See trial data + FDA approvals + patent timelines + biosimilar landscapes together. Make strategic decisions with complete regulatory context, not guesswork.
Geographic intelligence shows you market expansion, site additions, and regional competitive shifts the moment they happen, not weeks later when press releases go out.
Eliminate 2+ hours of daily manual checking. Automated 24/7 monitoring delivers critical competitor changes to your inbox before your competition even starts their morning research.
Connect AI assistants like Claude directly to your trial portfolio via MCP. Ask questions in natural language, request cross-portfolio analysis, and get answers grounded in your live regulatory data — no exports or copy-pasting required.
Export your entire regulatory intelligence portfolio — trials, drugs, devices, patents, safety data — in a single structured file with 22 cross-linked sheets, ready for AI agents, data pipelines, or team analysis.
Get answers to the most frequently asked questions about Clinicalister's competitive intelligence platform.
Our team is here to help. Get in touch with our sales team for personalized answers and to see how Clinicalister can transform your competitive intelligence.
Experience unified regulatory intelligence — connecting 590,300+ clinical trials with FDA and EMA drug and device data. Get priority access to all platform features including Drug & Device Intelligence and AI Analytics.
Ready to Automate YourCompetitive Intelligence?
Consolidate clinical trial research across 18+ databases into a single platform. Get automated alerts when competitors change strategy — and act on intelligence before your competition discovers it.
18+ Databases Unified
ClinicalTrials.gov, FDA, EMA, GUDID, and more — in one search
Near-Real-Time Monitoring
Automated change detection, refreshed throughout the day
Severity-Classified Alerts
Critical, High, and Medium priority — so you focus on what matters
Join the Beta
We're onboarding early users from pharma, biotech, and medical device teams. Request early access to see how automated competitive intelligence works with your workflow.