We're building the modern regulatory intelligence platform that pharmaceutical and biotech professionals deserve—automated, intelligent, and accessible.
Regulatory affairs professionals spend 30-60 minutes every single day manually checking FDA.gov, EMA.europa.eu, and Health Canada websites for updates. That's 5-10 hours per week—time that could be spent on strategic regulatory planning, submissions, or analysis.
We created RegulatoryAlerts to eliminate this manual busywork. By automating regulatory monitoring with intelligent summarization, we help pharmaceutical professionals stay informed without sacrificing their time.
Our goal is simple: Save you 5-10 hours per week while ensuring you never miss a critical regulatory update.
Professionals waste hours daily checking multiple government websites, searching through hundreds of pages for relevant updates.
Regulatory agencies publish hundreds of documents weekly. Finding what's relevant to your therapeutic area is like finding a needle in a haystack.
With manual monitoring, it's easy to miss important guidance changes, safety alerts, or competitive approvals that impact your work.
Our scrapers check FDA, EMA, and Health Canada websites 24/7, so you don't have to. We detect new updates within hours of publication.
Our system reads dense regulatory documents and creates clear bullet-point summaries, so you understand the impact in seconds instead of hours.
Configure your therapeutic areas and agencies. Get only the updates that matter to your work—delivered daily to your inbox.
Save 5-10 hours/week on monitoring. Focus on strategy, submissions, and analysis instead of manual website checking.
Stay current on GMP guidance, warning letters, and manufacturing regulations to maintain compliance systems.
Monitor IND requirements, clinical trial guidance updates, and safety reporting changes for protocol compliance.
Track multiple therapeutic areas and regions for diverse clients without multiplying your monitoring workload.
We're not a generic news aggregator. RegulatoryAlerts is purpose-built for pharmaceutical regulatory monitoring with therapeutic area filtering, agency-specific tracking, and regulatory document types.
Legacy RIM systems cost $10,000-$50,000/year with 6-month implementations. RegulatoryAlerts starts at $49/month with 2-minute setup. Enterprise features without enterprise bloat or pricing.
Most regulatory intelligence tools just aggregate links. We use advanced processing to read documents and create actionable summaries—so you understand the impact without reading 50-page PDFs.
Regulatory compliance is critical. We source all updates directly from official government websites and verify data integrity at every step.
We're honest about our capabilities, limitations, and pricing. No hidden fees, no misleading marketing claims, no surprises.
Your reading history, saved documents, and preferences are private. We never sell user data or use it for advertising purposes.
We actively listen to user feedback and ship improvements weekly. Your suggestions directly influence our product roadmap.
Start your free 14-day trial today. No credit card required.