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.

The FDA’s regulations and expectations for medical devices are designed to ensure that benefits outweigh the risks. In three months, the U.S.

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 U.S. Food and Drug Administration has flagged three of Philips' medical device facilities after inspections found they ...

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 ...

Stevanato Group S.p.A. continues expanding across global healthcare markets. The company strengthens its dual focus on biopharmaceutical solutions. Innovation and precision manufacturing support its ...

As healthcare systems work towards new sustainability goals, medical textiles have become a key focus for innovation.

The FDA has sent Philips a warning letter over three ultrasound and enterprise informatics facilities in the U.S. and the Netherlands.

A buck converter designed to help meet functional safety standards reduces the amount of necessary functional safety ...

Aluminum nitride is the fastest-growing material segment in the semiconductor ceramic packaging materials market in terms of ...

The CMOS Image Sensor Market is witnessing robust growth driven by escalating demand across automotive, consumer electronics, healthcare, and industrial automation sectors. Expanding adoption of ...

The report 'Semiconductor Ceramic Packaging Materials Market by Material (Alumina, Aluminum Nitride, Silicon Nitride, Silicon Carbide, Beryllium Oxide), Packaging Technology (Through-Hole Packages, ...