Global Vision Automated Proofreading Solutions
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Pharmaceutical Quality Control

The pharmaceutical challenge: The largest source of pharmaceutical product recalls is due to copy related errors on cartons, labels or inserts. In fact, over 51% of all product recalls in a six month period were the result of mislabeling according to statistics.

The accuracy of printed materials is key to the success of a pharmaceutical company. Imagine the severity of a decimal point accidentally moving from a .20 mg to a 2.0 mg?

GlobalVision understands your challenges. Strict regulations, multiple department participation, multilingual text, paper based inspections - all make proofreading a difficult and overwhelming task.


Industry Solutions: Pharmaceutical

 

Typical Applications Per Department:


Department Applications Suggested Products

Regulatory Affairs

 

Managing FDA Submissions and other forms of intense text or artwork management

 

DOCUPROOF
ARTPROOF

Graphic

 

Verifying:
Artwork revisions
Artwork vs. text
Artwork vs. print

 

DOCU-PROOF
ARTPROOF
SCANPROOF

Quality Control/Quality Assurance

 

Verifying approved Artwork vs. Print (Master vs. Sample Comparisons)

 

SCANPROOF

Labeling

 

Verifying Approved Artwork vs. Print (Master vs. Sample Comparisons)

 

SCANPROOF

Legal

 

Manage Contract revisions and changes to the “legal” section of text found on packaging

 

DOCUPROOF

Validation

 

Managing Documentation

 

DOCUPROOF

Pre-Press

 

Proof Vs. Customer Approved Artwork

 

ARTPROOF
SCANPROOF

Production

 

Printed Packaging vs. Approved Proof

 

ARTPROOF
SCANPROOF

Clinical trials

 

Checking clinical labeling vs. Approved item

 

ARTPROOF
SCANPROOF

Document Services

 

Managing multiple revisions and text heavy documents

 

DOCUPROOF

The Benefits of a GlobalVision Solution


global, vision, Globalvision, software, proofreading, montreal

GlobalVision is the only truly compliant supplier with complete lifecycle documentation including a Functional Requirements Specification, Detailed Design Specification, Unit Test Protocols, System Test Protocols, and Traceability Matrix. Furthermore, all GlobalVision products meet FDA 21 CFR Part 11/Annex 11 requirements. As a result, GlobalVision continues to successfully pass all major Pharmaceutical audits.

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Tailored to meet the needs of Regulatory Affairs, Marketing, Graphics, QA/QC, Product, Legal, all the way to Production. Our solutions are designed to secure your packaging workflow from end-to-end. Learn more about specific department applications.

global, vision, Globalvision, software, proofreading, montreal
global, vision, Globalvision, software, proofreading, montreal
Increase accuracy, decrease approvals, speed up time-to-market, and streamlines the proofreading processes.
global, vision, Globalvision, software, proofreading, montreal
global, vision, Globalvision, software, proofreading, montreal

 

global, vision, Globalvision, software, proofreading, montreal