CTWiseAPI – Programmatic access to clinical trial regulatory rules

Summary: CTWiseAPI provides instant REST API access to over 500 regulatory rules from FDA CFR Title 21, ICH Guidelines, EMA, and WHO. It enables semantic search and version tracking for clinical trial compliance, delivering results in under 200 milliseconds.

What it does

CTWiseAPI allows users to query specific regulatory rule citations related to clinical trials via a REST API, covering areas like 21 CFR Part 11, GCP compliance, informed consent, and IRB oversight. It supports semantic search to find relevant rules without exact keywords.

Who it's for

It is designed for pharmaceutical R&D, CROs, clinical operations teams, and biotech regulatory affairs professionals building or validating compliant clinical trial protocols.

Why it matters

CTWiseAPI eliminates manual document searches and expensive consultancy by providing fast, programmatic access to up-to-date regulatory requirements essential for clinical trial compliance.