Shawpak presents a new range of low-power, low-waste linear thermoforming machines to produce large, multi-component packs with snap features for the medical sector.
The FDA’s regulations and expectations for medical devices are designed to ensure that benefits outweigh the risks. In three months, the U.S.
The US Food and Drug Administration (FDA) has hit Philips with a warning letter after quality control shortcomings were uncovered at three of its medical device manufacturing sites.
Investing.com -- Koninklijke Philips N.V. (NYSE:PHG) stock fell 8% after the U.S. Food and Drug Administration (FDA) issued a warning letter to the company regarding multiple violations found during ...
To continue reading this content, please enable JavaScript in your browser settings and refresh this page. Preview this article 1 min The acquisition joins the local ...
The Food and Drug Administration is requesting public comment to get feedback on current, practical approaches to measuring and evaluating the performance of AI-enabled medical devices in the real ...
Supply chain resilience is now a defining factor for success in medical device manufacturing. With regulatory requirements, patient safety and quality assurance at stake, manufacturers must navigate ...
Today's pacemakers are about the size of a small matchbox, and future models are expected to shrink even further, becoming smaller than a grain of rice. Now, these devices, depending on the model, can ...
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