Streamline regulatory compliance, reduce manual work, and stay ahead of global changes — with an AI-powered software that’s fully customizable to your processes, documents, and risk profile.
An AI-driven, always-current library that monitors global health authorities like the FDA, EMA, MHRA, and more. Upload your SOPs, GxP policies, and quality documents to search, compare, and summarize regulatory insights in one unified platform.
AI collects and connects your SOPs, CAPAs, training logs, and other audit evidence in one place. Quickly generate checklists aligned with FDA, ISO, FAA, and other standards — so you're always ready for inspections, with less manual effort.
Monitor changes in clinical trial regulations, drug safety, labeling, pharmacovigilance, and GMPs. Receive personalized alerts and AI summaries to stay informed and never miss a critical update.
Automatically map internal SOPs and policies to global standards like FDA, EMA, EU MDR, and ISO. Identify documentation gaps, missing controls, and local compliance risks.
Easily adapt workflows, terminology, and document structures to align with your internal processes, regulatory model, and global compliance requirements.
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From drug development to market access, get a single view of compliance status across teams, geographies, and systems.
Monitor regulatory changes across the U.S., EU and Canada.
Developed by top AI engineers and compliance professionals to solve the real-world challenges of regulated industries.
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Unlike generic tools, our compliance platform is built to be fully customizable across industries. It adapts to your specific regulatory landscape, product types, and internal workflows — with AI models that can be configured to align with your unique compliance needs.
Our pharmaceutical compliance software covers FDA, EMA, ICH, MHRA, PMDA, and other major global health authorities. You can also add custom regional sources to match your operational footprint — making it a truly global pharma regulatory software platform.
Yes. Our solutions are fully customizable. You can upload internal SOPs, quality manuals, or validation documentation, and our AI maps them against external regulatory changes — an essential feature of any robust life science compliance software.
Yes. We follow enterprise-grade security practices, including end-to-end encryption, detailed audit trails, and role-based access controls. Your sensitive data is protected at every step — from document uploads to user activity.
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