The idea of pre-validated packaging sounds really good. Using packaging that has already undergone extensive testing seems ...

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 ...

AZCO Corporation announces the launch of the Securus VS610 Vertical Pouch Making Machine, a flexible, USA-made packaging ...

A new white paper urges medical device and combination product manufacturers to employ a solid package validation program as a means of preventing the failure of combination products. "FDA concerns ...

Inadequate process validation related to medical devices was cited more than 600 times by the US Food and Drug Administration (FDA) in 2013. In efforts to meet the agency’s standards, device ...

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 ...

Brazil’s health regulator Anvisa has ordered the suspension of several medical devices after identifying packaging failures that could compromise product safety. The decision adds to growing global ...

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 ...

The global poly peel sheets market is valued at USD 3.3 billion in 2026 and is projected to reach USD 9.8 billion by 2036, expanding at a 11.5% CAGR during the forecast period. Market growth is ...

Selbyville, Delaware, Jan. 21, 2025 (GLOBE NEWSWIRE) -- Medical Device Packaging Market was valued at USD 33.5 billion in 2023 and is projected to be worth USD 58.8 billion by the end of 2032, as per ...