AICA is set to redefine the work of regulatory compliance by reducing weeks of manual document review to hours of automated analysis. The platform proactively identifies compliance gaps before regulatory inspections occur, while generating reports that include specific corrective actions and regulatory references. Unlike traditional sampling-based audit approaches, AICA provides complete documentation coverage.
Built by regulatory practitioners for regulatory practitioners, AICA leverages AI trained specifically by FDA and ISO subject matter experts who understand the nuances of compliance requirements. The platform analyzes your policies, procedures, work instructions, and form templates against relevant CFR sections and ISO standards, providing the same level of expertise as hiring a team of regulatory consultants—but available 24/7 at a fraction of the cost.
The result is unprecedented visibility into your compliance posture. Instead of discovering gaps during high-stakes regulatory inspections, you can identify and address non-conformances during routine business operations.
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