CTWiseAPI
Clinical Trial Regulatory Rules API
CTWiseAPI launched on January 29, 2026 with 3 votes, #5,632 of 14,584 launches that month and more than 50% of that year's launches.
What it does
CTWise Regulatory Rules API delivers instant, programmatic access to FDA CFR Title 21, ICH Guidelines (E6 GCP, E8, E9), EMA regulations, and WHO guidance. Unlike document-based solutions, query specific rule citations in milliseconds via REST API. 500+ regulatory rules covering 21 CFR Part 11, GCP compliance, informed consent, and IRB oversight with semantic search and version tracking. Ideal for pharmaceutical R&D, CROs, and clinical operations teams building compliant protocols.
CTWiseAPI is a regulatory intelligence API that helps clinical trial professionals quickly search and understand compliance requirements across multiple regulatory sources.
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