Medical packaging sits at the intersection of materials science, sterilization, human factors, and global regulatory ...

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 ...

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 ...

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.

While some medical device manufacturers (MDMs) have in-house packaging lines and capabilities, many companies use a contract packager for their medical devices. Small-batch sealers are relatively ...

New and more stringent rules and quality regulations are emerging that are reshaping the future of many industries. However, one industry where this will have a ...

Medical device packaging is essential for ensuring sterility, safety, and integrity of medical instruments, implants, consumables, and diagnostic devices. It includes solutions such as pouches, trays, ...

LIMERICK, Ireland, Oct. 31, 2024 (GLOBE NEWSWIRE) -- kneat.com, inc. (TSX: KSI) (OTC: KSIOF), a leader in digitizing and automating validation and quality processes, is pleased to announce that a ...

ProMed, a leading contract manufacturer specializing in medical-grade silicone and plastic components, provides comprehensive support for medical device, pharmaceutical, and combination drug-device ...