RegulatoryFlow
AI-Powered Precision for Clinical Trial Excellence
Empowering Life Sciences with Text Engineering Innovation
From Evidence Matters' 24-Year Legacy in Clinical Trials Data Science to RegulatoryFlow – Your Modular SaaS Suite for Faster, More Accurate Regulatory Documentation
Building on our proven expertise in extracting insights from complex healthcare data (trusted by Stanford Medicine, VA, and 7,000+ users worldwide), RegulatoryFlow (RegFlow) revolutionizes workflows for CROs, pharma, and biotech. Navigate trial complexity, accelerate timelines, and ensure regulatory compliance with near-deterministic accuracy.
Overcoming Industry Challenges
In today's life sciences landscape, clinical trials face escalating complexity, costs, and regulatory scrutiny. RegulatoryFlow addresses these head-on.
Our flexible, modular platform customizes to your unique workflows, integrates seamlessly with tools like Microsoft Word, and lays the foundation for unified data sources – all while fostering effortless AI adoption.
Increasing Trial Complexity and Costs
Streamline data-to-document workflows to reduce errors and delays.
Accelerated Drug Development Timelines
Achieve 50-75% faster end-to-end protocols and study reports.
Evolving Regulatory Requirements
Confidently meet FDA/EMA standards with consistent, high-quality outputs.
Leveraging Cutting-Edge Tech
Integrate AI and Text Engineering for elevated efficiency, quality, and employee satisfaction.
RegulatoryFlow - Your Competitive Edge
Swift Customization
Tailored to your company's workflows, styles, and standards for rapid adoption.
Seamless Integration
APIs connect with familiar tools, ensuring smooth data flow across departments.
Modular Architecture
"A la carte" selection of modules to fit your needs – start small, scale effortlessly.
Bespoke Department Solutions
Enhance medical writing, regulatory affairs, and more with progressive AI enhancements.
Proudly partnering with Altasciences, a leading CRO, to advance AI-driven regulatory writing – as announced in our strategic collaboration.
Core Modules
SourceFlow
Revolutionizing TFL Data Transfer
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Reduces data transfer errors by 97-100%.
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Accelerates TFL-related tasks by 8-20x.
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Handles 90%+ of complex TFL files, including adaptive trials.
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Seamless Word integration for boosted efficiency in medical writing.
“After just a few uses, SourceFlow has reduced our TFL data transfer time by over 50%. It does things which no other tools we've tried can do, significantly improving the efficiency and accuracy of our medical writing workflows.”
Senior Medical Writer, Mid-Sized CRO
Draft Insights
Automated In-Text Study Results
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Automatically generates in-text study results, saving time and ensuring accuracy.
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Maintains consistency across Clinical Study Reports (CSRs).
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Integrates effortlessly with existing processes for regulatory specialists.
Upcoming Modules and Roadmap
Empowering Life Sciences with Text Engineering Innovation
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RegulatoryFlow
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