Vision – Print Inspection

Vision - Print Inspection

The FDA stipulate that all medical device and pharmaceutical labels must be suitably checked for accuracy against errors… that’s where PRISYM 360 Vision can help.

Printing errors in your processes arise for many reasons. Taking a risks within the quality of your labels isn’t an option, at worst it can lead to harm to patients and even loss of life. You need a solution that brings the control, operation and traceability under one umbrella.

PRISYM ID has developed Vision, a module for our label management software, PRISYM 360, to provide end-to-end label print inspection set up, test, management and audit capabilities. This unique centralized solution is fully integrated with industry-leading print inspection hardware solutions that offer high accuracy, in-line print verification technology.

  • Removes risk through automated inspection.
  • Ensures regulatory compliance by meeting inspection requirements and logging exceptions in a secure audit trail.
  • Reduces cost by minimizing effort.
PRISYM Vision Datasheet Vision Inspection Systems Posted in: Achieving Regulatory Compliance, Business Analysis, Clinical Trials, Data Sheet, Increasing The Operational Efficiency, Information Technology, Medical Device, Operations & Labeling, Overcoming The Technical Challenges, Pharmaceuticals, Project Managers, Regulatory & Compliance, Supply Chain -

We have developed PRISYM 360 Vision, a module for PRISYM 360 label management software, to provide complete print inspection set up, test and management functionality. 

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VISION RESOURCES

A Clear Vision whitepaper 1 - A Clear Vision: Developing the Right Strategy to assure Compliant Labeling Inspection A Clear Vision: Developing the Right Strategy to assure Compliant Labeling Inspection Posted in: Whitepaper, Achieving Regulatory Compliance, Increasing The Operational Efficiency, Information Technology, Medical Device, Operations & Labeling, Overcoming The Technical Challenges, Reducing Risks, Regulatory & Compliance -

The continual tightening of regulation around the packaging and labeling of medical devices has so far failed to stimulate a transformation of labeling infrastructure and approach among global device manufacturers.

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