Scanflow’s AI visual inspection system helps pharmaceutical manufacturers ensure packaging integrity, verify label accuracy, and detect visual anomalies across production, filling, and secondary packaging lines, supporting compliant, traceable, and efficient quality operations.
Quality control in pharmaceutical production must meet stringent regulatory standards and zero-tolerance thresholds for error. Yet manual inspections still dominate label verification, packaging checks, and defect detection making quality highly dependent on operator consistency and prone to fatigue-driven oversight.
Visual inspection errors account for a significant portion of packaging-related recalls
Mislabeled or unverified products can lead to regulatory non-compliance and safety risks
Automated visual inspection improves batch-level traceability and reduces deviation handling time
- Scanflow reads and verifies batch codes, expiry dates, drug names, and serial numbers on blister packs, cartons, and bottles to ensure legibility, presence, and accuracy before release.
- The system inspects for defects such as seal irregularities, torn foils, smudged print, or misaligned labels, catching deviations before they reach downstream packaging or dispatch.
- Scanflow integrates into packaging and serialization lines to monitor presence, alignment, and label conformity of each unit, helping meet traceability and DSCSA or EU FMD compliance requirements.
Blister Pack Label Verification and Print Inspection
Vial and Bottle Packaging Inspection
Final Carton Inspection and Batch Release Readiness
info@scanflow.ai 
+1 (213) 283-7163 
