With regards to patient safety, we highlight that nearly all the considered breakthrough devices are classified by the FDA as Class 2 (moderate risk; 51/81, 63 percent) or Class 3 (highest risk ...

While generative artificial intelligence ("GenAI") has the potential to fundamentally change health care, it presents unique risks and ...

Integra Lifesciences recently received an FDA warning letter pertaining to quality systems issues at several facilities.

The Food and Drug Administration (FDA) is being sued in two lawsuits after releasing its Final Rule on Laboratory Developed ...

Eclypsium security researchers have uncovered UEFI vulnerabilities in the Illumina iSeq 100 DNA sequencer, but the broader ...

A man has appeared in court charged with drug supply offences after police found mobile phones in a South Staffordshire ...

Metabolic medicines dominated life sciences headlines in 2024, a trend expected to continue into the new year. Other things ...

Tech giant Apple, responsible for the ubiquitous iPhone and other devices like iPads and Apple Watches, has agreed to pay a ...

US FDA approves AVITA Medical’s RECELL GO mini disposable cartridge to treat smaller wounds: Valencia, California Friday, December 27, 2024, 18:00 Hrs [IST] AVITA Medical, Inc., ...

One manufacturer was forced to pay a large settlement earlier this year after it recalled a number of CPAP devices. The FDA said Zepbound ... and Wegovy, this class of medications has become ...

Oregon is kicking off 2025 with new laws to stop drug use on public transportation, reduce the cost of prescription drugs and ...

“We are very excited to receive FDA clearance for the innovative SIMEOX 200 therapy ... and marketing innovative best-in-class respiratory therapy devices used to deliver care to patients suffering ...