--> --> -->

Blogs

01
Aug 2024

How VeriPac Flex Systems Enhance Quality Assurance in Dry-Filled Pouch Packaging?

How VeriPac Flex Systems Enhance Quality Assurance in Dry-Filled Pouch Packaging?

In the pharmaceutical industry, ensuring the integrity of packaging is crucial for maintaining the safety, efficacy, and quality of products. Dry-filled pouch packaging, commonly used for its convenience and cost-effectiveness, requires stringent quality assurance measures to protect the contents from contamination, moisture, and physical damage. One advanced solution that has significantly enhanced quality assurance in this area is the VeriPac Flex System. This system employs advanced technology to provide non-destructive package integrity testing, ensuring that each pouch meets the highest standards of quality and reliability.

Importance of Packaging Integrity

In today’s increasingly complex and globalized supply chains, maintaining packaging integrity has become more challenging and essential than ever. The rise of e-commerce and the demand for longer shelf lives necessitate advanced packaging solutions and rigorous testing protocols. Consequently, the importance of packaging integrity extends beyond mere containment—it plays a vital role in ensuring consumer satisfaction, fostering brand loyalty, and driving industry innovation. This is especially crucial in sectors such as pharmaceuticals, and food and nutrition, where the packaging serves not only as a container but also as a barrier against contamination, degradation, and tampering.

Effective packaging integrity assures products remain safe, effective, and of high quality throughout their shelf life, thereby safeguarding consumer health and maintaining trust. Moreover, it helps in complying with stringent regulatory standards, reducing economic losses due to product recalls and waste, and supporting sustainability efforts by minimizing environmental impact.

Dry-Filled Pouch Package Inspection Using VeriPac Flex

VeriPac FLEX Systems are versatile inspection solutions designed for pouches and flexible packaging. They provide a clear PASS or FAIL result along with quantitative data on leak rates. Renowned for their exceptional sensitivity, reliability, and ease of use, these systems work seamlessly across various package formats and sizes without needing adjustments or tooling changes. With multiple configurations available for both the inspection instrument and test chamber capacity, VeriPac FLEX Systems meets a wide range of package specifications and sensitivity needs. They accommodate everything from small sachets and stick packs to large bulk pouches and bags.

Utilizing the ASTM method for vacuum decay leak testing (F2338) and endorsed by the FDA, VeriPac FLEX Systems conforms to recognized standards for package integrity testing. By replacing subjective and wasteful destructive testing methods, they offer a more efficient and cost-effective alternative. The vacuum decay leak testing technology employed by VeriPac systems delivers rapid returns on investment compared to traditional destructive methods like water baths or blue dye tests. These systems reliably detect critical packaging failures while providing valuable insights into the packaging process. VeriPac FLEX technology has also been fully automated for production line inspection.

Why VeriPac Flex stands out for dry-filled pouches?

  • Deterministic, quantitative test method
  • Cost-effective with rapid return on investment
  • Non-destructive, non-subjective, no sample preparation
  • Supports sustainable packaging and zero-waste initiatives
  • Test multiple packages in a single test cycle
  • ASTM test method and FDA standard
  • USP < 1207> compliant

In conclusion, the VeriPac Flex System significantly enhances quality assurance in dry-filled pouch packaging through its state-of-the-art non-destructive testing technology. This system leverages advanced vacuum decay methods to detect leaks and ensure the integrity of packaging, offering numerous advantages for pharmaceutical companies. Integrating the VeriPac Flex System into the quality assurance framework ensures that pharmaceutical companies can maintain high standards of product integrity and safety. This not only safeguards patient health but also strengthens regulatory compliance and operational efficiency, ultimately enhancing the company’s market position and consumer trust.

Readmore...
vacuum decay leak testing, quality assurance, non-destructive testing
246

Popular Blogs

Tags

CCIT for Pharmaceutical Package Integrity

Jul 23, 2021   |   3174

Container Closure Integrity Testing of pharmaceutical packaging ensures that the products remain intact throughout its shelf life or until it reaches the end user.

Techniques Involved in Leak Testing Vials

Sep 06, 2022   |   2980

Most common methods for leak testing vials include MicroCurrent HVLD Technology, Helium Leak Testing and Vacuum Decay Technology.

Why is Seal Integrity Testing of Medical Device Packaging Important

Jul 29, 2021   |   2835

For sterile medical devices, seal integrity testing ensures product efficacy, shelf-life stability, and microbial sterility. Airborne Ultrasound technology is a non-destructive Container Closure Integrity test method, capable of examining seal quality for defects.

A Guide to MicroCurrent HVLD Technology

Aug 05, 2021   |   2738

In the case of parenteral drug product containers, HVLD technology is ideal for CCI testing in cases where packaging is less conductive than the liquid within.

Everything You Need to Know About Vacuum Decay Technology

Sep 09, 2022   |   2728

Vacuum Decay technology is the ideal non-destructive solution for container closure integrity determination for many package formats.
Popup