` VeriPac LPX

PTI Packaging Technologies and Inspection

VeriPac LPX

Fully automated package quality inspection systems for 100% inline testing.

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The VeriPac LPX Series is PTI’s line of fully automated package quality inspection systems for 100% inline testing. The LPX enables enhanced automated testing that provides a high level of confidence in packaging line performance. The LPX is a practical and reliable solution to the problems associated with performing infrequent testing, allowing for process-related quality issues to be recognized and corrected sooner rather than later.

The VeriPac LPX features a dynamic robotic design, tailored to fit your production requirements. The LPX Series are scalable, modular solutions to meet production line demands. This adaptable platform provides reliable automated handling of a variety of packaging formats. Applications for LPX automation range from flexible packaging to rigid containers, and parenteral products.
 
Vacuum decay is a deterministic method to provide reproducible and reliable results for leak testing of high-risk package applications. It can be applied to a wide variety of package formats and product types. The test involves placing a package in a test chamber, applying vacuum, and monitoring the vacuum level for any change, which would indicate the presence of a leak. Test chambers are configured according to package specifications, test sensitivity and handling requirements.
 
The VeriPac LPX is modular providing the flexibility and versatility of easy changeover for testing different size packages on the same system. Sensitivity and reliability go hand in hand with CCI testing. The VeriPac LPX 430.8S is the next generation automated inspection system for container closure integrity testing of parenteral products. Automated for 100% testing or batch release, the VeriPac 430.8S is an eight-station dual chamber design robotic testing platform for pre-filled syringes and vials, testing products filled with lyophilized product, small molecule liquids and Water for Injection (WFI). 

 • Automated testing enables the highest level of container quality assurance

• Deterministic, quantitative test method
• ASTM Test Method F2338 and FDA standard, ISO 11607
• Distinct PASS/FAIL results
• Highly accurate test results - low false positives and false negatives
• High Signal Noise Ratio (SNR) for peak sensitivity and reliability
• Non-destructive, non-subjective, no sample preparation
• Pick-and-Place option back into the production line
• Auto reject option of defects removed from the production line
• USP <1207> compliant

Inspection Platform Rotary and in-line configurations
Package Type Flexible and rigid containers
• Pouches
• Stick packs and sachets
• Cups, trays, bottles
• Vials and pre-filled syringes
Package Materials Tyvek®, paper, foil, film, poly, aluminum, plastic, glass, laminated
materials
Test Configuration Automated for production line applications
Test Method Vacuum Decay – Single or Dual Transducer PERMA-VAC Technology
Operator Interface HMI Color Touch Screen
Data Collection • View on HMI screen and electronic data collection
• PTI-ETHOS, CFR 21 Part 11 capability
Test Frame Enclosure • Stainless steel frame
• Lexan protective shielding for moving systems
Test Chamber Test Chamber design and number of test stations determined by
package specifications, test sensitivity and handling speed
Pick & Place Robotic Arm (4-axis or 6-axis) application dependent
Recognized Test Method • ASTM F2338 vacuum decay technology
• USP<1207> chapter guidance
• Annex 1
Options Validation Qualification Package (IQ/OQ)



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