Does your packaging operation still depend on paper?
Digitize batch records, QA approvals, rejection logs, and packaging planning — with ALCOA+ traceability from day one.
The problem
Manual batch records
Paper-based batch documentation that takes 72 hours to reconstruct for an audit.
72hrs
reconstructing a batch
Informal QA approvals
Quality approvals by email or WhatsApp with no auditable evidence.
0
formal records
Unrecorded rejections
Rejected batches with no root cause traceability or pattern analysis.
0%
preventive analysis
Planning without data
Packaging planning based on estimates, not actual historical data.
0
data for planning
How we solve it
Digital batch record with electronic signatures
Every batch stage is recorded with electronic signature, timestamp, and ALCOA+ traceability.
QA approval workflows with escalation
Formal approvals with levels, time limits, and automatic escalation.
Automatic rejection logging
Every rejection is documented with cause, responsible party, and corrective actions.
Packaging dashboard
Real-time visibility of batches, performance, and quality metrics.
Results
100% ALCOA traceability
85% less time on documentation
Audit-ready in minutes
Preventive rejection analysis
Why SYNOV
Platform with active pharma clients in production and direct experience in Latin American regulation and packaging processes.
Want to see how it works in your operation?
Schedule a free consultation and we'll show you the platform with a case from your industry.