20+ Years of AI-Curated Expertise

    rEGS — Regulatory Knowledge Graph

    Regulatory Knowledge Graph

    A structured regulatory knowledge graph that organizes FDA, EMA, ICH, and GxP requirements into machine-readable intelligence. The data foundation that powers DAIN.

    DAIN reasons about regulations. rEGS stores regulatory intelligence.

    20+ years regulatory expertise
    Powered by DAIN intelligence
    Expert escalation available

    Our Evolution

    Do You Know Your rEGS?

    From our first vision in 2011 to today's AI-powered platform—we've always believed in putting all your rEGS in one basket.

    v2011
    The Beginning

    "Put all your rEGS in one basket"

    Our original vision: a customizable mobile and web app bringing regulations to you—anytime, anywhere. We saw the need for consolidated regulatory intelligence long before AI made it truly possible.

    • Static document libraries
    • Manual search & navigation
    • Human expertise only
    v2025
    The Future is Now

    rEGS — AI-First

    The vision fulfilled: AI curated from 20+ years of BIGGSB industry expertise, delivering instant answers trained on global regulatory frameworks with human expert escalation.

    • AI-powered natural language queries
    • Real-time regulatory updates
    • AI speed + human expertise

    Platform Capabilities

    Everything You Need for Regulatory Intelligence

    Purpose-built for life sciences professionals who need fast, reliable regulatory guidance.

    AI-Powered Analysis

    Get instant answers to complex regulatory questions using advanced AI trained on FDA, EMA, and global regulatory frameworks.

    Expert-Backed Accuracy

    Every AI response is grounded in real regulatory documents and can be escalated to human experts for validation.

    Real-Time Intelligence

    Stay ahead with up-to-date regulatory guidance, including recent FDA announcements and policy changes.

    Document Analysis

    Upload SOPs, protocols, or regulatory submissions for AI-powered review and compliance checking.

    Multi-Jurisdiction Coverage

    Navigate FDA, EMA, PMDA, TGA, and other major regulatory bodies from a single platform.

    Team Collaboration

    Share insights, track regulatory queries, and maintain an audit trail for your entire organization.

    Use Cases

    Regulatory Questions, Answered in Seconds

    From pre-IND strategy to post-market surveillance, rEGS handles the full spectrum of regulatory intelligence needs.

    Pre-submission regulatory strategy
    Clinical trial compliance questions
    GxP and quality management guidance
    Post-market surveillance requirements
    Medical device classification
    Pharmacovigilance obligations
    CMC documentation requirements
    Import/export regulations

    Simple Process

    AI Speed. Human Expertise.

    01

    Ask Your Question

    Type your regulatory question in plain language—no jargon required.

    02

    Get AI Analysis

    Our AI searches regulatory databases and returns a sourced, comprehensive answer.

    03

    Escalate If Needed

    Request human expert review for complex or high-stakes decisions.

    Ready to Transform Your Regulatory Workflow?

    rEGS supports BiggsB consulting engagements. Talk to us about how structured regulatory intelligence could support your project.