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 ...
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 ...
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.
ProMed, a leading contract manufacturer specializing in medical-grade silicone and plastic components, provides comprehensive support for medical device, pharmaceutical, and combination drug-device ...
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 ...
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 ...
When its FDM process alone was inefficient for creating prototypes, Oertli 3D printed positive molds to serve as a thermoforming template for the Mayku Multiplier. In the realm of advanced medical ...
The government has notified the Legal Metrology (Packaged Commodities) Amendment Rules, 2025, introducing specific provisions for medical device packaging that align with the Medical Devices Rules, ...
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