Pharmacovigilance & Drug Safety
Put a safety signal in context across the class: who is running what, which populations are enrolled, and which trials stopped.
What this team sees first.
A Sankey flow shows where trials end up by sponsor type. In Phase 3 atopic dermatitis, 23 of 245 industry trials stopped.
Every use case below opens with its signature chart and a recommended set of supporting views, chosen from 91 chart types.
Built for: Pharmacovigilance Signal Lead, PV, Drug Safety, Benefit-Risk, Pharmacovigilance.
Industry runs 245 of 278 Phase 3 atopic dermatitis trials; 23 of those stopped
ClinicalTrials.gov API, pulled 16 Oct 2026: interventional Phase 3 atopic dermatitis trials, all years. Stopped = terminated, withdrawn or suspended. Government includes NIH, federal, other government, networks and individual investigators.
Ranked by stakes, centrality, reach, frequency and data fit.
Each use case ships with an executive brief, a detailed dossier and a recipe that builds the board in one click.
- PV-01
#38Signal detection context
Check whether an adverse event has been observed in related programs across the compound class.
For: Pharmacovigilance Signal LeadForest plotAnalysis of Competing Hypotheses matrixKPI / metric snapshot panel - PV-02
#48Periodic safety update report (PSUR) support
Compile a complete list of studies using your compound or class for the PSUR clinical overview.
For: PV / Aggregate Reporting LeadComposition / share-of-inventory chartForest plotKPI / metric snapshot panel - PV-03
#49Safety population benchmarking
Understand what populations are typically enrolled to inform your expected safety profile.
For: Drug Safety / PV ScientistForest plotComposition / share-of-inventory chartHeatmap / matrix - PV-11N
#50MedDRA-harmonised class safety landscape
A normalised, class-wide safety view across trials and labels using MedDRA and ATC coding.
For: Pharmacovigilance Signal LeadBullseye100% stacked barComposition / share-of-inventory chart - PV-04
#71Benefit-risk framework enrichment
Quantify total patient exposure across an indication to support the benefit-risk narrative.
For: Benefit-Risk / PV LeadComposition / share-of-inventory chartForest plotHeatmap / matrix - PV-05
#72Background incidence rate research
Find studies measuring disease natural history and event rates for adverse-event context.
For: Pharmacovigilance / Epidemiology LeadForest plotComposition / share-of-inventory chartHeatmap / matrix - PV-06
#84Patient sub-population risk monitoring
Identify trials studying vulnerable populations in your class to inform safety monitoring.
For: Drug Safety / PV ScientistTimelineProbability-impact bubble chartComposition / share-of-inventory chart - PV-07
#86Long-term follow-up study identification
Find long-term extension/follow-up studies offering durability and late-onset safety data.
For: PV / Long-Term Safety LeadComposition / share-of-inventory chartForest plotTimeline - PV-08
#88Risk minimization measure benchmarking
See what risk-minimization measures regulators have already required for comparable products.
For: Drug Safety / RMP LeadFeature-by-feature alignment chartComposition / share-of-inventory chartForest plot - PV-09
#89Post-authorization safety study (PASS) design
Find existing PASS-style designs to use as templates or to identify collaborating sites.
For: PV / RWE Study LeadComposition / share-of-inventory chartForest plotPoint / site map with catchment radii - PV-10
#90Expedited reporting threshold calibration
Understand what events have triggered early study stops to calibrate reporting thresholds.
For: PV / Risk LeadKPI / metric snapshot panelComposition / share-of-inventory chartForest plot
Ask the registry a pharmacovigilance question.
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Bring one pharmacovigilance question to a pilot.
Eight weeks, one programme, success criteria agreed up front.