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Unified clinical intelligence

Clinical trial data.
Structured for decisions.

Search 1M+ trials, follow drug pipelines from discovery to approval, and monitor global regulatory movement in one place.

Coverage

Primary registries and regulatory agencies your team checks every day.

ClinicalTrials.govEU CTRFDAEMANMPA+3 more

Platform Scale

1M+

Clinical Trials

Indexing all major global registries, updated daily.

30K+

Drug Programs

100K+

home.platformStatApprovals

12+

Regulatory Agencies

10K+

Companies Tracked

195

Countries Covered

Daily

Data Updates

How It Works

From question to insight in minutes

A streamlined workflow to find answers faster.

01

Search & Discover

Enter your research question or browse by therapeutic area, company, or trial ID.

02

Analyze & Compare

Use AI-powered tools to analyze protocols, compare drugs, and identify trends.

03

Generate Reports

Create comprehensive reports with citations, ready for team sharing or presentation.

04

Stay Updated

Set alerts for trials, drugs, or companies to receive real-time notifications.

Use Cases

Built for life sciences professionals

Whether you're conducting research, sourcing deals, or tracking regulations.

Clinical Researchers

Find relevant trials, analyze protocols, and identify collaboration opportunities.

  • Protocol comparison
  • Site identification
  • Competitor analysis

BD & Investors

Track pipelines, monitor approvals, and identify licensing opportunities.

  • Pipeline intelligence
  • Deal flow tracking
  • Market analysis

Regulatory Affairs

Monitor global approvals, compare labels, and track regulatory trends.

  • Approval tracking
  • Label comparison
  • Agency insights

Medical Affairs

Research evidence, track publications, and support medical strategy.

  • Evidence synthesis
  • KOL identification
  • Publication tracking

Trusted by Researchers Worldwide

Medical professionals, pharmaceutical companies, and research institutions use MedPath to accelerate clinical trial discovery and drug intelligence.

50K+
Monthly Searches
195
Countries Covered
12+
Data Registries
99.9%
Uptime

Frequently Asked Questions

What data sources does MedPath use?
MedPath aggregates data from ClinicalTrials.gov, WHO ICTRP, EudraCT, and 12+ regulatory agencies including FDA, EMA, NMPA, TGA, and Health Canada. All data is updated daily.
How does the AI research assistant work?
Our AI analyzes trial protocols, regulatory documents, and scientific literature to provide insights. All AI-generated content includes source citations for verification.
Is the data on MedPath free to access?
Basic search and trial information is free. Pro and Team plans unlock advanced features like AI research, data export, and priority support.
How often is the data updated?
Clinical trial data is updated daily from primary registries. Regulatory approval data is updated as announcements are made. News is aggregated in real-time.

Start your research today

Join research teams using MedPath for clinical intelligence.

No credit card required • Free tier available