Vivos' cost-cutting initiatives also led to a $1 million or 27% year-over-year reduction in operating loss, versus the third quarter of 2023. For the nine months ended September 30, 2024 operating ...

The U.S. Food and Drug Administration's ("FDA") new advisory committee on digital health is set to examine its approach for evaluating and ...

PCCP empowers medical device manufacturers to implement updates and improvements without the traditional ... Leveraging ...

After a career as a corruption investigator, Aaron Narva had an idea for a startup in the age of LLM AI: help hospitals ...

Top Capa Software Company for Corrective Action Management In today’s fast-paced business environment, Corrective and ...

Successful MDSAP certification confirms compliance with Health Canada and U.S. FDA quality management system requirements, replacing FDA audit and inspection if required Health Canada and U.S. FDA ...

As the FDA continues to develop and solidify its guidance and regulations on AI, medical device manufacturers should prepare ...

They are not allowed to make medical decisions by themselves, and they can't diagnose patients or decide how to treat them. “They’re not qualified to do it," Stern said. "We run a high risk ...

The flaw allows attackers to gain control over affected devices, potentially accessing sensitive functions remotely. Samsung has acknowledged the flaw and issued an October security patch to fix it.

The Association of Indian Medical Device Industry (AiMeD) warns that imported refurbished devices are often inaccurately labelled, posing a significant risk to patient safety. The lack of clear ...

A new commentary found that power plants' use of these devices saved up to 9,100 lives ... to air pollution-related public health risk anymore in the US, thanks to federal policies that ...