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Nitin Bhattileft a comment
@david_firouzbakht Thanks for the upvote! Would love to hear more about what excited you about this product. Thank you.
CTWiseAPIClinical Trial Regulatory Rules API
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.
CTWiseAPIClinical Trial Regulatory Rules API
Nitin Bhattileft a comment
I'm Nitin, founder of OrchestraPrime. I built CTWise for a specific problem in clinical trials. **The Problem:** When pharma companies and CROs develop clinical trial protocols, they need to ensure compliance with FDA regulations, ICH guidelines, and other regulatory requirements. Today, this means: - Manually searching PDF documents - Paying consultants $500/hour for regulatory expertise -...
CTWiseAPIClinical Trial Regulatory Rules API