Regulated & Industry Verticals
Clinical Trials
Studies, EDC, eTMF, IRT, and eConsent.
Study management, an EDC / eCRF designer, site payments, an eTMF with completeness tracking, IRT / RTSM, eConsent and eCOA / ePRO.
What's inside
11 capabilities in Clinical Trials — every one a real surface in the product, not a roadmap item.
- Overview
- Studies
- EDC / eCRF Designer
- Site Payments
- eTMF
- TMF Documents
- TMF Completeness
- IRT / RTSM
- IRT Studies
- eConsent
- eCOA / ePRO
See it in action
Not a dashboard tour — the actual working screens in Clinical Trials, on live demo data.
Who it's for
Clinical operations running trials end to end.
Connected to
Same database, same records — Regulated & Industry Verticals works as one.
Food & BeverageFSMA 204 traceability and food-safety plans.CosmeticsMoCRA end to end — registration to adverse events.Device R&DDesign controls, risk files, DHF/DHR, and UDI.Pharma & BiologicsCompound registry, IND programs, and PPQ.Life SciencesPortfolio, pipeline, and requirements tracing.Regulatory AffairsSubmissions, commitments, and HA meetings.PharmacovigilanceICSRs, signals, aggregate reports, and MDR.R&DELN, LIMS, biobank, and assays.NonprofitDonors, grants, funds, and Form 990 prep.
See Clinical Trials on your own data.
Book a demo