ERP for Pharmaceutical: GMP Compliance, Batch Traceability, and Expiry Management

Pharmaceutical manufacturing operates under the most stringent quality regulations in the world. Every raw material, every process step, and every finished goods batch must be traceable — and your ERP is the system of record.

Batch Traceability from RM to FG

Infuro ERP records every material movement with lot numbers — from raw material receipt through weighing, granulation, compression, coating, and packaging to the finished goods batch.

Expiry Date Management

The system blocks issuance of materials within 30 days of expiry (configurable per material class) and auto-generates destruction requests for expired stock.

Electronic Batch Records

CFR Part 11-compliant e-signatures and audit trails mean every process deviation is logged with the user, timestamp, and reason — audit-ready at all times.

LIMS Integration

Infuro integrates with laboratory information management systems. QC results auto-update the batch status — approved lots released to dispatch, rejected lots quarantined — without manual intervention.