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Stop relying on manual checks and passive monitoring. PV Verify actively validates your critical compliance emails with a human-in-the-loop process, generating audit-ready certificates every day.
Your server status says "Online," but that doesn't mean emails are arriving. In the pharmaceutical world, "I didn't get the email" is not a valid excuse to the FDA.
Common silent failure modes include:
Missing a report can lead to huge fines and, more importantly, patient harm.
We move from Passive Assumption to Active Verification. We don't just "ping" the server; we ensure the safety net is actually open.
Every day, our system automatically injects a benign Verification Token into your safety intake channel (e.g., safety@company.com).
A designated PV staff member must open the email and click the secure link. This proves the inbox is accessible and monitored by a real person.
Successful verification generates a SHA-256 hashed PDF Certificate ("Birth Certificate" for that day).
If it fails, we immediately escalate to IT before a real safety report is lost.
PV Verify is designed to alignment with Regulatory Authorities (FDA, EMA, MHRA) requirements for robust systems.
Provides documentary evidence of system availability for inspections.
Certificates are stored in a WORM (Write Once, Read Many) compliant environment.
Detects failures *before* a genuine Adverse Event is missed.
External 3rd party validation of internal IT infrastructure.
Demonstrate control over your intake channels for any historical date.
Eliminate the risk of silent technology failures endangering patients.
Join the compliance teams who rely on PV Verify to ensure their safety net is always open.
Start Free TrialNo credit card required for pilot access.