Smarter Pharmaceutical Proofreading & Quality Control Starts Here
For over 30 years, GlobalVision has been the trusted pioneer in pharmaceutical quality control—helping life sciences teams eliminate errors and accelerate time-to-market by speeding up regulatory, labeling, promotional, and quality assurance workflows.
Trusted by the world’s leading life sciences teams
Why Leading Organizations Trust Our Pharma Inspection Solutions
Drive Error-Free Content and Packaging Inspections
Expedite Review Cycles and Time-to-Market
Protect Your Bottom Line With Automation
Safeguard Patient Safety Through Flawless Content and Labeling
Biogen Optimizes Artwork Development With GlobalVision
Savings are attributed to reduced misprints, missed manufacturing slots, and reprocessing costs.
When Zero Tolerance For Errors is the Standard.
In addition to catching errors, GlobalVision helps you ensure that intended edits have accurately been applied to your files by referencing your annotations!
Regulatory Requirements? Consider Them Covered.
FDA Pharmaceutical Packaging Requirements
- Ensure content integrity in SPLs (XML and PDF formats)
- Support 21 CFR Part 11 Compliance with built-in security and audit trails
- Review promotional content against FDA-approved submission documents
- Check packaging against approved structured labelling content
EMA Regulatory Labeling
- Validate braille readability and Marburg Medium Font Standard compliance
- Automate comparisons between the QRD document and final artwork
- Ensure accuracy of SmPCs and PILs across digital and print formats
- Validate multilingual labeling content using EMA-approved structures and built-in dictionaries
- Prepare for Annex 11 audits with validated inspection workflows
Health Canada Regulatory Requirements in Pharmaceutical Packaging
- Built-in Canadian English and French dictionaries for accurate bilingual artwork inspection
- Compare final proofs to PLL-compliant master documents to catch layout or content deviations
- Ensure alignment with approved Product Monographs (PMs) through document-to-document comparison
- Create new file versions of changes for PAAB submissions
MHRA Regulatory Labeling Requirement Specifications
- Automated inspections of SmPCs and PILs, regardless of region
- Comparison of regulatory-approved content against final packaging or promotional materials
- Support for English-only labeling and validation of layout, font, and copy
- Annotated file copies from inspection reports ready to submit
“[...] GlobalVision offerings are the most well-rounded and usable that I have seen. Especially for life sciences labeling (artwork), such as pharma, biologics, & medical devices. [...]. The amount of risk that a company carries using a fully-manual/human process is hard to quantify for an ROI statement. But ask this question— how much does a recall cost? That is a quantifiable cost. How much does patient harm/death cost? That number is beyond quantification. But, just calculating the number of man hours this will save in proofing alone can easily justify the ROI of [GlobalVision]. Especially for companies that market in multiple languages.”
Need to send files for inspection directly from Veeva Vault?
Take advantage of our Verify and Veeva Vault integration.
We’ve Got You Covered. From Lab To Launch.
Catch all errors, review intended changes, and boost efficiency.
Regulatory Inspection
Ensure error-free submissions with automated checks across SPLs, SmPCs, and e-labels. Support ODPD, 21 CFR Part 11, and Annex 11 with audit trails and validated workflows.
Labeling Asset Proofreading
Catch content and artwork errors across cartons, leaflets, and e-labeling files. Compare files pixel by pixel to ensure accuracy, compliance, and production-ready packaging.
Promotional Materials Reviews
Streamline MLR and PAAB workflows by flagging content changes, claim mismatches, and layout issues. Maintain compliance from concept to final promotional asset.
Incoming Quality Control (IQC)
Verify supplier files on receipt by comparing them to approved specs. Prevent costly errors and delays with automated inspections of packaging and print components.
Automate Pharma Content and Packaging Inspections
FAQs
What is packaging quality control in the pharmaceutical industry?
Packaging quality control ensures that all packaging components like cartons, labels, leaflets, and blister packs are inspected for accuracy, completeness, and compliance before reaching patients. GlobalVision automates this process by catching errors in text, artwork, barcodes, and braille to help teams stay audit-ready and avoid costly recalls.
What does a pharmaceutical quality inspection typically include?
A quality inspection in pharma involves verifying that content, packaging, and labeling meet strict regulatory and safety standards. GlobalVision empowers QA teams to automate inspections across multi-format files, catching deviations in real time to ensure data integrity, accuracy, and compliance.
What should a pharmaceutical inspection system be able to do?
A reliable inspection system should detect inconsistencies in regulated content including text, graphics, barcodes, and layout across every document and packaging stage. GlobalVision offers an end-to-end platform that integrates into pharma workflows to ensure inspection accuracy without slowing reviews.
How to improve pharmaceutical packaging inspection accuracy?
Automated inspection systems like GlobalVision reduce human error by detecting issues in design files, print-ready proofs, and physical packaging. They help verify content alignment with regulatory approvals, avoid mislabeling, and maintain production speed while supporting GxP and 21 CFR Part 11 compliance.
How does GlobalVision help maintain pharmaceutical data integrity?
Pharmaceutical data integrity ensures that information is accurate, complete, and unaltered throughout the product lifecycle. GlobalVision supports this by logging every inspection, maintaining version history, and offering traceable audit trails aligned with ALCOA+ principles and global regulatory requirements.
How do inspection systems support pharmaceutical packaging workflows?
Inspection systems play a critical role in pharmaceutical packaging by detecting errors in text, artwork, layout, barcodes, and braille before packaging goes to print or production. GlobalVision enables teams to automate these inspections, ensuring content accuracy, regulatory alignment, and packaging integrity—while reducing manual effort and the risk of costly recalls.
