What's newPurple Book + ClinicalTrials.gov updates

Regulatory intelligence as an API

Access FDA press releases and MedWatch alerts, drug applications and submissions, DailyMed labels, ClinicalTrials.gov studies, advisory committee calendars, device approvals and recalls, and the FDA Purple Book — in one consistent API with clean JSON and powerful range filters.

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Coverage that matters

End-to-end coverage across the biomedical lifecycle

Coverage across FDA, ClinicalTrials.gov, DailyMed, Federal Register, industry news (Drugs.com), and research preprints (bioRxiv/medRxiv). Endpoints backed by ingested, normalized datasets. All endpoints share consistent filtering operators, pagination via `limit` + `next_token`, and predictable JSON response envelopes.

Production endpoints

44

Ready for mission-critical workflows

Coverage areas

14

Normalized datasets spanning research to market

Live data sources

15

Trusted regulatory, research, and market feeds

Coverage areas
Drug ApplicationsClinical TrialsDrug SafetyDrug LabelsDevicesAdvisory CommitteeRecallsPurple BookMarket IntelligenceNewsOrange BookPDUFA+2 more
Explore datasets

By researchers for researchers

Made for scientists, developers, startups, and healthcare innovators

Clean, normalized data from trusted sources with real-time updates and comprehensive coverage.

Standardized JSON/REST.
Clean, normalized data from trusted sources with consistent API responses across all endpoints.
Real-time Updates.
FDA alerts, clinical trials, and drug approvals as they happen with instant data synchronization.
Comprehensive Coverage.
From drug discovery to market surveillance - complete biomedical data ecosystem in one API.
{
  "data": [
    {
      "title": "FDA Approves Leqembi for Treatment of Alzheimer's Disease",
      "published_date": "2024-01-15T14:30:00Z",
      "category": "drug-approval",
      "description": "FDA grants accelerated approval for new Alzheimer's treatment...",
      "url": "https://www.fda.gov/news-events/press-announcements/...",
      "meta_slug": "fda-rss-press-releases",
      "meta_fetched_at": "2024-01-15T15:00:00Z"
    },
    {
      "title": "FDA Issues Safety Alert for Contaminated Eye Drops",
      "published_date": "2024-01-14T09:15:00Z", 
      "category": "safety-alert",
      "description": "FDA warns consumers to stop using certain eye drop products...",
      "url": "https://www.fda.gov/safety/medical-product-safety-information/...",
      "meta_slug": "fda-rss-press-releases",
      "meta_fetched_at": "2024-01-14T16:00:00Z"
    }
  ],
  "total": 1247,
  "meta": {
    "source": "FDA RSS Press Releases",
    "last_updated": "2024-01-15T15:00:00Z"
  }
}

Use cases

Built for analysts, BD, and builders

Never miss a catalyst. Unify regulatory events, exclusivity, and clinical signals—then automate the alerts.

Drug Discovery

Track compounds through clinical development phases, monitor competitive landscapes, and identify potential drug targets using comprehensive clinical trial data.

Market Research

Monitor pharmaceutical industry trends, analyze drug approval patterns, and stay ahead of regulatory changes with real-time FDA data.

Academic Research

Access comprehensive datasets for meta-analyses, systematic reviews, and large-scale studies with consistent, clean data formats.

Investment Analysis

Combine financial and scientific data to make informed investment decisions in biotech and pharmaceutical companies.

Turn regulatory chaos into APIs

PDUFA dates, approvals, exclusivity, biosimilars, and trials—normalized with provenance.

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