Automated Quality Control Tools for Regulatory Affairs

GlobalVision helps ensure content accuracy across entire legal and regulatory departments.

1000+

Customers Worldwide

4.3

Capterra Rating

4.2

G2 Crowd Rating

Automated Quality Control Tools for Regulatory Affairs

GlobalVision helps ensure content accuracy across entire legal and regulatory departments.

1000+

Customers Worldwide

4.3

Capterra Rating

4.2

G2 Crowd Rating

Keep Files Compliant With FDA Guidelines as They Move Through Regulatory Departments

Ensure that all copy documents are 100% accurate for internal revisions and regulatory submissions.

  • Stop errors from being created as content is transcribed from reference materials
  • Automatically inspect text-heavy documents with character-to-character precision
  • Ensure that the correct FDA information is formatted and applied to labels and packaging

Manage Localization by Ensuring that Content is Accurate For Use in Foreign Markets

Protect labels and packaging from unintended errors to ensure compliance in all markets where products are sold.

  • Get products to market faster by eliminating long delays caused by manual quality control
  • Automatically compare text and spelling in over 30 foreign languages
  • Check final regulatory documents against approved content to make sure they’re consistent before moving to graphics

Products

Text inspection App icon
 
Text
Inspection
Spelling inspection App icon
 
Spelling
Inspection
Graphics inspection App icon
 
Graphics
Inspection

Products

Meet Compliance
and Data Integrity Requirements

GlobalVision’s automated quality control tools have been developed to meet compliance and data integrity requirements for use in the pharmaceutical and life sciences industries.

ISO 9001:2015
CERTIFIED

ANNEX 11
COMPLIANT

21 CFR PART 11
COMPLIANT

AUDIT TRAIL
MODE

CGMP
COMPLIANT

GAMP 5
COMPLIANT

Transform Your Regulatory Team’s Quality Control Process With GlobalVision