Select a tool below to process your regulatory documents with AI-powered analysis.
Detect and mask PII/PHI in clinical trial data. DPDP Act 2023 compliant. Supports 47+ entity types across 12 Indian languages.
Convert regulatory filings, CSRs, and SAE narratives into concise CDSCO-ready summaries with MedDRA classification.
Validate submissions against SUGAM/MD Online requirements. Flag missing fields, classify severity, detect duplicates.