Pharmaceutical Manufacturing
PackProof QA
AI-powered artwork inspection for pharmaceutical excellence.
Automated packaging artwork inspection — text, graphics, barcode, color, and Braille — catching discrepancies before they reach print, with the inspection depth of leading global artwork QC platforms.
- FDA 21 CFR Part 11
- EU Annex 11
- WHO GMP
- PIC/S GMP
- ISO 19351 (Braille)
Core Modules
The same inspection depth as leading global artwork QC platforms, built to plug into your existing artwork and document workflows.
Inspection Technologies
AI Text & Copy Comparison
Compare approved copy documents against print-ready files to catch missing words, punctuation, font, and formatting changes.
Graphics & Pixel-Level Compare
Pixel-to-pixel comparison of artwork and print proofs against the approved master, surfacing even the smallest visual deviation.
Barcode & QR Grading
Locate, decode, and grade barcodes and QR codes against ANSI, CEN, and ISO standards, flagging contrast and quiet-zone issues.
Braille Inspection
Verify Braille translation, dot spacing, and height against the Marburg Medium font standard and ISO 19351 for EU medicinal packaging.
Quality & Compliance Checks
OCR-Based Content Validation
Extract and verify on-pack text — dosage, batch details, warnings, regulatory copy — against approved reference content.
Multi-Language Spell Check
Spell-check across dozens of languages with support for custom and medical dictionaries specific to your product portfolio.
Color Inspection
Detect color shifts and registration issues between approved artwork and production proofs before they go to press.
Deviation & Discrepancy Reporting
Automatically generate structured discrepancy reports the moment an inspection fails, ready to route into QMS Pharma.
Workflow & Traceability
Version & Revision Control
Track every artwork revision with a clear approval history and side-by-side change comparison.
Annotation & Markup
Mark up, comment, and route proofs for review with a full collaboration trail across QA, regulatory, and vendors.
Electronic Signatures & Audit Trail
Every inspection, approval, and rejection is logged with a timestamped, attributable audit trail.
Batch Inspection History
Retrieve the complete inspection record for any batch, SKU, or market variant in seconds during an audit.
Ready For Compliance
Why CoreMind Vision
Enterprise-grade capability, without the enterprise-only price tag or year-long rollout.
Full Inspection Stack
Text, graphics, barcode, color, and Braille inspection in one platform — not a single-purpose tool that leaves gaps in coverage.
Minutes, Not Days
Automated comparison replaces manual proofreading cycles that can take a QA reviewer hours per artwork file.
Plugs Into Your Workflow
Built to work alongside your existing artwork management, document management, or PLM system rather than replacing it.
Regional Pricing & Support
Enterprise-grade inspection accuracy at a price point designed for regional manufacturers, not just global CPG enterprises.
Precision Inspection At Production Speed
Manual artwork proofreading is slow and error-prone. PackProof QA combines computer vision and OCR to inspect packaging artwork with a level of consistency manual review can't match.
- Cut artwork approval cycles from days to minutes
- Reduce the risk of mislabeling and packaging-related recalls
- Standardize inspection criteria across every product and market
- Keep a defensible, timestamped record for every approved artwork
- Free QA reviewers to focus on genuine discrepancies, not routine checks
PackProof QA FAQ
Barcodes and QR codes are graded against ANSI, CEN, and ISO standards. Braille is checked against the Marburg Medium font standard and ISO 19351 for EU medicinal packaging compliance.
PackProof QA supports multi-language spell checking with custom and medical dictionaries, so product-specific and regulatory terminology is recognized correctly.
Yes. PackProof QA is built to work alongside existing artwork management, document management, and PLM systems rather than requiring you to replace them.
A structured discrepancy report is generated automatically and can be routed directly into a QMS Pharma deviation for investigation and disposition.