Regulated & Industry Verticals
Pharmacovigilance
ICSRs, signals, aggregate reports, and MDR.
Case intake and workflow for ICSRs, safety-signal detection, aggregate reports, MDR, and literature monitoring.
What's inside
7 capabilities in Pharmacovigilance — every one a real surface in the product, not a roadmap item.
- Overview
- ICSRs
- Safety Signals
- Aggregate Reports
- MDR
- Literature
- Case Workflow
See it in action
Not a dashboard tour — the actual working screens in Pharmacovigilance, on live demo data.
Who it's for
Pharmacovigilance and safety teams managing case volume.
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.Clinical TrialsStudies, EDC, eTMF, IRT, and eConsent.R&DELN, LIMS, biobank, and assays.NonprofitDonors, grants, funds, and Form 990 prep.
See Pharmacovigilance on your own data.
Book a demo