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Powerful Features for Regulatory Professionals

Everything you need to automate regulatory intelligence monitoring, save time, and never miss critical FDA, EMA, or Health Canada updates.

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24/7 Automated Monitoring

Our scrapers check FDA CDER, FDA CBER, EMA, and Health Canada multiple times daily, ensuring you never miss critical regulatory updates.

  • Checks agency websites every few hours
  • Detects new guidance documents, approvals, warnings
  • Automatic categorization by document type
Automated Document Summaries

Our intelligent system reads dense regulatory documents and creates clear, actionable bullet-point summaries so you understand the impact in seconds.

  • Advanced processing handles complex PDFs
  • Extracts key requirements, deadlines, changes
  • Highlights therapeutic areas affected
Intelligent Filtering

Configure your therapeutic areas, agencies, and document types. Only see what matters to your work—eliminate the noise.

  • Filter by 15+ therapeutic areas
  • Select specific agencies (FDA, EMA, HC)
  • Choose document types (guidance, approvals, warnings)
Daily & Weekly Email Digests

Personalized email summaries delivered on your schedule. Review updates over morning coffee instead of manually checking websites.

  • Choose daily or weekly delivery
  • Timezone-aware scheduling
  • Mobile-responsive email design
Instant Telegram Alerts

For premium subscribers: critical regulatory updates delivered instantly to your phone via Telegram. Never miss urgent changes.

  • Mobile-first instant notifications
  • One-tap access to full documents
  • Configure urgency thresholds
Save & Organize

Bookmark important updates, add private notes, create custom tags, and organize documents by project or indication.

  • Unlimited saved documents
  • Private notes and annotations
  • Custom tagging system
Advanced Search

Full-text search across all regulatory updates. Filter by date range, agency, therapeutic area, and document type.

  • Search entire document content
  • Multi-dimensional filtering
  • Export search results to CSV
Reading History & Analytics

Track which updates you've reviewed, identify trends over time, and measure engagement with regulatory intelligence.

  • Mark as read tracking
  • Trend analysis dashboards
  • Export history for reporting
Team Collaboration (Enterprise)

Share saved updates, collaborate on notes, and maintain centralized regulatory intelligence for your entire team.

  • Shared team workspaces
  • Collaborative annotations
  • Role-based access control

Manual Monitoring vs. RegulatoryAlerts

FeatureManual ApproachRegulatoryAlerts
Automated Monitoring❌ 30-60 min/day checking websites✅ Automated 24/7 monitoring
Smart Summaries❌ Read 50-page PDFs yourself✅ Intelligent bullet-point summaries
Therapeutic Area Filtering❌ Manual Ctrl+F through docs✅ Automatic filtering
Multi-Agency Coverage❌ Check 4+ websites daily✅ Single unified feed
Mobile Alerts❌ Desktop-only access✅ Telegram instant alerts
Historical Archive❌ Limited search✅ Full searchable archive

Integrations & API Access

REST API (Enterprise)

Integrate regulatory updates directly into your internal systems, dashboards, or compliance platforms.

  • • Programmatic access to all updates
  • • Webhook notifications
  • • Custom integration support
Export Capabilities

Export search results, saved documents, and reading history for compliance documentation and reporting.

  • • CSV export for Excel
  • • PDF summaries
  • • Bulk export options

Experience All Features Risk-Free

14-day free trial. No credit card required. Full access to all features.

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Automated regulatory intelligence monitoring for pharmaceutical and biotech professionals. Track FDA, EMA, and Health Canada updates seamlessly.

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