Blogs CCIT

18
Nov 2022

Powdered Dairy Products Package Testing Using VeriPac FLEX Series

Powdered Dairy Products Package Testing Using VeriPac FLEX Series

The sensitivity of a test method is necessary for several reasons, but it is most crucial in ensuring the final product is of high quality. Powdered dairy products (milk powders, infant formula, protein-based powders) are kept in a modified environment to avoid spoilage and maintain the nutritional value of the product throughout its shelf life. Before usage, the product will quickly deteriorate due to oxygen and moisture intrusion, affecting the flavor and texture and finally converting any desirable commodity into a liability. The quantity and impact of oxygen ingress depend on a number of variables, and it will occur in the presence of tiny leaks. Leaks as small as 10 microns will have an immediate impact on the product for smaller packaging types. Current conventional test techniques are completely insufficient for identifying such defects, leaving manufacturing operations exposed to severe quality variations. Applying techniques with greater sensitivity provides the highest level of quality assurance, rather than just locating minor leakage.

Ensuring Dairy Products Package Integrity with VeriPac FLEX Series

For pouches and other flexible packaging, VeriPac FLEX systems are versatile non-destructive package inspection systems. These are available in a variety of configurations for the leak test instrument and the test chamber capacity, with solutions to accommodate small format sachets and stick packs up to bulk size pouches and bags. This is done to accommodate different package specifications and test sensitivity requirements. The Food and Drug Administration (FDA) has recognized the ASTM technique for Vacuum Decay leak testing (F2338) defined in ISO 11607 as a consensus standard for pharmaceutical package testing. This approach is used by VeriPac FLEX Systems.

VeriPac inspection systems are the best alternative for destructive testing since they eliminate the subjectivity of test results and reduce the waste and costs associated with these techniques. Comparing Vacuum Decay leak testing technology to destructive techniques like the water bath or blue dye leak test, it has been found to offer a quick return on investment. The VeriPac test provides reliable critical packaging failure detection and useful packaging process insight.

Technology Overview

The VeriPac test instrument is attached to the appropriate FLEX chamber based on the size range of the packages. Depending on the application, two VeriPac systems combined with the FLEX chamber offer varying levels of leak detection capabilities. The Integrated Flexible test chamber (IFC) is designed for low-headspace sachets or stick packs. Depending on the package size and requirements, the Drawer Style test chamber (D-Series) comes in two common sizes, the Small (D) or Large (DXL). Custom designs are capable of being produced for huge package forms and bulk products. The manner in which the package is tested is the unique difference with VeriPac FLEX systems. Multiple packages can also be tested in a single test cycle.

VeriPac FLEX Series Benefits

  • Non-destructive, deterministic and quantitative test method.
  • Does not require any sample preparation.
  • Perform a single test cycle for several packages.
  • USP < 1207> compliant.
  • Promote zero-waste initiatives and sustainable packaging.
  • Makes the inspection and validation procedure easier.
  • Reliable and repeatable outcomes.
  • FDA standard and ASTM test methods.
  • Inexpensive with a quick return on investment.

Flexible packaging is highly susceptible to routine microleaks that reduce shelf life and contaminate dairy proteins, considered a very high-risk product. VeriPac FLEX is an optimal solution for powdered dairy products package integrity testing. They offer a definite PASS or FAIL in addition to quantitative data corresponding to a leak rate.

Readmore...
vacuum decay leak testing, pharmaceutical package testing, container closure integrity testing, cci technologies, container closure integrity
186
16
Nov 2022

A Complete Guide to Helium Leak Detection Technology

A Complete Guide to Helium Leak Detection Technology

The quality of the product and the maintenance of the sterile barrier against outside forces are both critically dependent on the packaging. Even a tiny hole in the packaging might allow moisture, reactive gases, or other dangerous elements to enter the product, limiting its ability to heal. Additionally, a contaminated pharmaceutical product can cause serious health issues to the user, making it more of a threat than a treatment. Maintaining Container Closure Integrity is extremely important due to the sensitive nature of pharmaceutical products.

Container Closure Integrity testing is a leak detection technique for determining how well sterile barriers are maintained against external contamination. These tests may be roughly divided into probabilistic and deterministic test methods. Manufacturers choose deterministic test procedures since they provide precise, guaranteed quantitative results. One such test method is helium leak detection technology.

Helium Leak Detection Technology Overview /h2>

Helium leak testing is the method of identifying leaks in various enclosed or sealed systems by utilizing helium as a "tracer" gas and measuring the concentration of the gas as it leaves due result of a leak. A vial is a good example of package system. A pre-filled syringe, a foil pouch, and a cold form blister card are some other examples. Each of these package types is intended to keep the pharmaceutical product contained while preventing the entry of potentially dangerous environmental contaminants like dust, bacteria, or even gases. Helium leak testing method can evaluate these package types. It is a highly efficient approach for finding leaks that provide quantitative leak rate data considerably beyond the capabilities of existing leak testing techniques.

The following describes how helium leak detection works: The package is initially vacuumed and helium-filled. The amount of helium escaping the package is then measured quantitatively and expressed as a leak rate using a helium leak detector. The technique is also ideally suited for packaging line setup and validation, failure analysis, tool qualification, monitoring product quality, and package design.

Why Use Helium as a Tracer Gas?

There are several reasons why helium is considered an ideal test gas for finding leaks.
  • Deterministic seal quality inspection method that produces quantitative outcomes.
  • Regardless of color, transparency, print, surface polish, or porosity, this method works for all material types and combinations.
  • Non-destructive and non-subjective test technique that does not require any sample preparation.
  • Technology may be used for 100% online final pouch seal defect detection.
  • Seal quality inspection results are repeatable, reproducible and reliable.
  • Cost-effective solution for testing seal integrity and seal analysis that characterizes the overall quality and uniformity of the seal.

Helium Leak Detection Merits

  • Practical and sensitive flow-based leak test method.
  • Enables the discovery of extremely small microleaks.
  • Detects leaks with sensitivity levels as low as 1x10-10 mbar L/sec.
  • Helium is a non-explosive, non-toxic and non-destructive tracer gas.
  • Applicable across package design, failure analysis, packaging line setup and validation.
  • Faster test cycle reduces cost and total processing time.

Applications of Helium Leak Detection

  • Vials
  • Pre-filled syringes
  • Blister packs
  • Combination products
  • Bottles
  • Foil pouches

Helium leak detection is the best option for evaluating the inherent integrity of specific primary container closure systems of pharmaceutical and parenteral products. It is a commonly used technology in early stage pharmaceutical package development and component compatibility evaluation. In comparison to other leak test techniques, helium leak testing has the highest level of sensitivity, making it the most used CCI test method. In accordance with ASTM F2391, helium leak detection is a widely used method in the pharmaceutical industry.

Readmore...
container closure integrity testing, helium leak detection, cci technologies, helium leak testing, container closure integrity
183

Popular Blogs

Tags

Why Microcurrent HVLD is the most preferred CCI technique for Parenteral Product Leak Testing ?

May 24, 2021   |   1302

Microcurrent HVLD is one of the most preferred container closure integrity testing method for Biological & Parenteral Product Leak Testing

Airborne Ultrasound Technology for Efficient Medical Device Package Inspection

May 28, 2021   |   1230

Package integrity testing of medical devices is vital to ensure the products maintain quality and sterility throughout its shelf life or until it is administered.

Evaluating Relevance of Seal Quality Inspection in Medical Device Industry

Jun 02, 2021   |   1166

Evaluating quality and integrity of package seal is an important criteria for medical device package inspection. Airborne Ultrasound technology allows non-destructive seal quality inspection of multiple device packages.

Vacuum Decay Technology Raising Standards for Pharmaceutical Package Testing

Jul 15, 2021   |   1021

Vacuum Decay technology is a non-destructive leak testing method, capable of evaluating a wide of pharmaceutical packaging formats.

Pharma Package Testing CCI of High-Risk Pharmaceuticals

May 21, 2021   |   997

Pharma package testing now has become an integral part of the pharmaceutical industry when it comes to the package integrity of high-risk pharmaceuticals.
COPYRIGHT 2022, CCIT, ALL RIGHTS RESERVED PRIVACY AND COOKIES TERMS OF USE
Popup