PTI Launches VeriPac LPX 100% In-line Automated Package Leak Detection Solutions at Interphex in Booth 3119
Hawthorne, New York (October 15, 2021) – PTI will launch the VeriPac LPX Series of fully
automated package quality inspection systems for 100% inline testing at Interphex, October
19-21, 2021 at the Jacob Javits Convention Center in New York City in Booth 3119.
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 package integrity testing to rigid
containers and container closure integrity testing of parenteral products.
“VeriPac LPX enables enhanced automated testing that provides a high level of confidence in
packaging line performance, stated Scott Audette”, VP Sales & Marketing. “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. VeriPac vacuum decay technology has been proven to be the most sensitive, most reliable
vacuum-based leak test method on the market, backed by decades of dependable performance
in the pharmaceutical, biologics and medical device industries.”
Sensitivity and reliability go hand in hand with Container Closure Integrity Testing (CCIT). The VeriPac LPX 430.8S is the next
generation automated inspection system for CCI of Parenteral products. Automated for 100%
testing or batch release, the VeriPac 430.8S is an eight-station dual chamber design robotic
test platform for pre-filled syringes and vials, testing products filled with lyophilized product,
small molecule liquids and Water for Injection (WFI).
VeriPac LPX systems utilize PTI's vacuum decay technology, an ASTM Test Method F2338,
developed using the VeriPac platform.
- Test method is recognized by the FDA as a consensus standard
for package integrity testing.
- Listed in ISO 11607 and USP Chapter <1207> guidance.
VeriPac LPX Benefits
- 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
Additional PTI automated technology platforms:
- E-Scan MicroCurrent HVLDmc for parenterals
Force Decay for blister packs and low headspace packaging
- Airborne Ultrasound for pouch seal quality inspection
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