To help teams fully realize these benefits, the following at-a-glance reference reinforces the core ASTM packaging standards ...

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 ...

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.

Regulators increasingly want medical device manufacturers to begin with a more precise understanding of their product's ...

Inadequate process validation is one of the most common issues leading to warnings from the US Food and Drug Administration (FDA). It may also be the most difficult to address, according to Max ...

Laboratory-based design verification testing (DVT) of combination products and medical devices must be performed to demonstrate that the device meets the performance requirements that were set in the ...

Cranston, R.I.-based health care packaging supplier Nelipak Corp. is expanding with a new, 60,000-square-foot packaging production facility in Grecia, Costa Rica. Nelipak has operated in Costa Rica ...