01
What it does
- Open a nonconformity file
- Check lot traceability
- Assemble an admin regulatory pack
- Prepare a deviation or vigilance sheet
Role · Product quality and compliance
An AI employee to frame lots, gaps and product files.
It prepares nonconformity files, checks lot traceability and assembles administrative packs — including pharma admin — with no clinical decision.
A clear mission. Controlled execution.
02
What it checks
- Lot / product / date consistency
- Completeness of required documents
- Quarantine / release statuses
- Your QMS thresholds and rules
03
Your tools
- QMS / eQMS
- ERP and traceability
- Quality DMS
- Regulatory portals
Start with one process
A real process, framed from day one.
Quality = evidence and lots. Pharma admin = complete files — never medication advice.
- Nonconformity handling
- Lot and date checks
- Pharma administrative file
- Signal preparation (no clinical decision)
Role-specific reasoning
Each role has different trade-offs. Here is how an AI employee reasons in this context — not a generic template.
No. In quality, “almost” does not exist in the system of record. The AI employee applies your criteria: if a check is missing or a threshold is crossed, the lot stays as a documented deviation / quarantine.
Unblocking production is a signed human decision. The agent documents; it does not bypass.
Let’s discuss your first process
Verisav Agents runs on your server. We scope one role, your tools and the right level of control.