RegIntel is VelorQ's AI Agent for pharmaceutical regulatory affairs. It continuously ingests guidance from FDA, EMA, and CDSCO, structures CTD and eCTD dossiers from your source documents, and flags gaps before submission — built for regulatory teams who can't afford a missed deadline or an outdated reference.
FDA, EMA, and CDSCO guidelines, unified in one agent.
CTD and eCTD modules, structured automatically.
Agency changes flagged the moment they're published.
Every submission deadline, tracked without a spreadsheet.
Missing sections caught before you submit, not after.
Every change logged, timestamped, and reviewer-ready.
Dossiers & guidelines, parsed automatically
Cross-checked against current requirements
CTD/eCTD modules generated automatically
Deadlines & agency changes, monitored live
Continuous intelligence, not a one-time check — RegIntel runs this cycle for every active submission.
Hours of manual cross-checking, done in minutes.
Fewer human errors in every submission.
Every filing tracked and flagged automatically.
A complete, timestamped trail for every document.