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.

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 ...

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.

The Director General of the National Agency for Food and Drug Administration and Control, NAFDAC, Prof. Mojisola Adeyeye, has expressed the hope that the nation would manufacture vaccines before she ...

In boardrooms across the globe, a fundamental shift is taking place. Regulatory compliance, once viewed as a back-office ...

Explore high-paying trade jobs that don't require a college degree. According to the Bureau of Labor Statistics, many offer ...

BANGKOK: Prime Minister Anutin Charnvirakul used the Asean and Apec summits to personally urge US President Donald Trump to lower tariffs and improve trade terms for Thailand, while Deputy Prime ...

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