In February 2026, our team visited a leading packaging manufacturer’s R&D laboratory in Finland to review their experience with the Labthink C840H Integrated Residue on Evaporation Testing System. Continue reading
Integrating Residue on Evaporation testing into your Performance Qualification is not just a regulatory hurdle—it is a cornerstone of quality design. By understanding the relationship between OM and E&L, manufacturers can ensure their packaging provides a safe, inert environment for the products they protect. Continue reading
The stability and shelf life of an eye drop container are directly determined by the packaging s ability to maintain a sterile barrier and provide high-resistance to oxygen transmission and moisture loss. By utilizing high-precision barrier testing and container-closure integrity (CCI) validation, manufacturers can prevent active ingredient degradation and microbial ingress, ensuring products remain safe until the period when eye drops expire. Continue reading
The pharmaceutical industry strategically transitioning toward sustainable practices, through the integration of Post-Consumer Recycled (PCR) materials and lightweight packaging strategies.
However, in a highly regulated environment, "eco-friendly" cannot come at the expense of "regulatory compliance," these shifts require precise quantification of Oxygen and Water Vapor Transmission Rates (OTR/WVTR), as recycled polymers and thinner walls can significantly alter the barrier and mechanical properties of the packaging material and integrity of the container closure system.
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Designing a "greener" pharma pack requires a sophisticated balance between environmental responsibility and the uncompromising requirements of sterile medical packaging. In the pharmaceutical industry, sustainability is achieved not only through end-of-life recyclability but also through material efficiency (source reduction) and waste prevention enabled by rigorous shelf life testing. Continue reading