Command Center
One place to see workload, urgent review items, source health, and next actions.
Pharmacovigilance workflow platform
Apexity brings literature monitoring, signal context, ICSR intake, label review, and audit trails into one evidence-linked safety workspace.
Product-event evidence ready for triage
ICSR candidate summary and source context
Label context, expectedness support, decision log
Why it matters
Literature, FAERS, labels, cases, signals, and reports often live in separate tools and queues. Teams lose time reconciling source provenance, duplicate records, evidence snippets, and reviewer decisions.
Apexity gives safety leaders one operating layer for source-grounded review and controlled handoffs.
Product
Apexity turns source monitoring, evidence extraction, reviewer routing, and audit-ready outputs into connected workflows.
One place to see workload, urgent review items, source health, and next actions.
Review source-derived ICSR candidates before promotion into operational case workflows.
Monitor PubMed, Europe PMC, PMC OA, and manual uploads with review queues and source-to-case extraction.
Review public signal context, disproportionality views, supporting evidence, and caveats around spontaneous reports.
Compare labels, support expectedness review, and capture reviewer decisions with source-backed context.
Create line listings, review records, exports, governance views, and traceability for audit preparation.
How it works
Bring in literature, labels, selected public safety context, and manual uploads.
Structure records, reconcile duplicates, and maintain source provenance.
Surface product-event matches, evidence spans, ICSR likelihood, and reviewer explanations.
Queue items to the right reviewer with disposition, comments, and role-based actions.
Generate traceable review records, line listings, handoff packages, and audit trails.
Solutions
Intake, triage, queue management, SLA visibility, and handoffs.
Evidence review, ICSR likelihood, medical assessment support, and signal context.
Listedness workflows, label comparison, and source-backed decisions.
Audit trails, reviewer actions, provenance, and controlled workflows.
Scheduled monitoring, live search, full-text resolution when legally loaded, manual upload fallback, and deduplication.
Platform
Apexity connects source monitoring, AI-assisted evidence extraction, reviewer routing, and governance controls without replacing PV judgment.
PubMed, Europe PMC, PMC OA, and manual uploads.
Product/event matching, evidence spans, ICSR likelihood, and reviewer explanations.
Queue routing, disposition, candidate creation, and case handoff.
Human review, audit history, role-based actions, and source provenance.
Governance
Apexity keeps review work structured from intake to disposition, so teams can move faster without losing traceability.
Prioritized queues, evidence context, and clean disposition flows.
Outputs stay linked to source records, evidence spans, and provenance.
Actions, comments, decisions, and handoffs are captured as work happens.
Trusted by leading pharmaceutical companies worldwide




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Open the Celltrion pilot workflow for literature surveillance, signal review, case intake, and label/listedness workflows.
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