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 ...

Insights from the SPMC (Sterilization Packaging Manufacturers Council) on a risk-based sustainability assessment model ...

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 ...

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 ...

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.

Dublin, Sept. 29, 2025 (GLOBE NEWSWIRE) -- The "An Introduction to ISO 11607 - Packaging for Terminally Sterilized Medical Devices Training Course (Nov 17, 2025)" training has been added to ...

In this free webinar, learn how medical devices benefit from modern digital validation strategies. Attendees will learn how digital validation builds confidence and removes redundancy. The featured ...

DUBLIN--(BUSINESS WIRE)--The "Global Medical Device Packaging Market, by Product Type, by Application, by Material Type, by Packaging Type, by End-user, Estimation & Forecast, 2017-2030" report has ...

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, ...

LONDON--(BUSINESS WIRE)--The medical device packaging market is expected to grow by USD 3.14 billion during 2020-2024. The report also provides the market impact and new opportunities created due to ...