Figure 1. (click to enlarge) Effect of temperature on seal strength. The green bars represent samples created using low temperature. The orange indicates packages created using the high-temperature ...

In order to assist manufacturers in complying with the ISO 11607 standard requirements for packaging process development, equipment manufacturers are increasingly incorporating validation software and ...

Sterilization is, of course, a fundamental requirement in the medical field. Here are four common reasons for failing a sterile barrier packaging validation test, presented by MDDI Online. 1.

From my product development experiences, entering into Design Verification and Design Validation is always bittersweet. Exciting because yes, to get to Design Verification means that we have ...

Though it is widely understood that medical devices are developed under rigorous quality controls, it is less widely known that the packages that house them are also subjected to rigorous validation ...

BOULDER, Colo., Aug. 14, 2025 /PRNewswire/ -- Medical device developers seeking efficient, accurate packaging and distribution testing have a new option with the opening of Boulder BioLabs. Part of ...