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Automated monitoring
Regulatory sources are checked around the clock, on a running schedule, not when someone remembers to look.
NFA & Regulatory Intelligence
Automated monitoring, powered by AI.
Built by ZenithPV, watching regulatory sources for pharmacovigilance teams around the clock.
Run in progress
Synthetic demonstration06:04US FDAUS
Matched06:03EMAEU
Running06:02MHRAGB
Matched06:01Health CanadaCA
Failed06:05PMDAJP
ClosedHow it works, in brief.
Three parts, always in that order: monitoring, analysis, then ZenithPV's oversight.
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Regulatory filings are read for signals like hepatotoxicity as soon as they publish.
AI-assisted analysis
AI reads every document first, matching what's relevant to your products before a person has to search for it.
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F-24817PendingConfirmed
Expert oversight
ZenithPV's pharmacovigilance expertise stands behind every alert, so what reaches you is worth acting on.
Two kinds of change worth watching.
Zenith Insights watches for what pharmacovigilance teams can't afford to miss.
NFA
Watching
- FDAWatching
- MHRARecall posted
Foreign action notifications
When a regulator abroad takes action on a product (a recall, a label change, a safety communication), it can trigger a reporting obligation at home. Zenith Insights watches for those actions as they happen.
RI
Safety labelling guidance
v3.22024
v3.3Updated
Regulatory intelligence
Guidelines and policies change too. Zenith Insights tracks updates from health authorities so your team is never working from an outdated version.
See it on your products.
Log in if you already have an account, or book a demo to see Zenith Insights in action.