A seasoned FDA compliance and regulations expert says you can watch for these major ways health intelligence may change for the public.
The future of medical devices has much potential, but they also have risks related to cybersecurity. In 2024, we saw the first full year of the Food and Drug Administration’s (FDA) new guidance ...
Today, the U.S. Food and Drug Administration (FDA) issued a safety communication to raise awareness about cybersecurity vulnerabilities in Contec CMS8000 patient monitors and Epsimed MN-120 patient ...
The FDA has recalled Mercury Medical’s ... ventilation and has been designed with in-line flow control. The recall affects devices used for pediatric patients weighing less than 10 kg.
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The vulnerabilities allow unauthorized users to remotely control the monitors and stop them working as intended, the FDA said, for example by denying access to the devices or corrupting the data. A ...
NCT05014568 and NCT05032859), which found that more patients treated with tapinarof achieved vIGA-AD success than those who received the vehicle control cream. In December, the FDA approved Nemluvio ...
That’s how it became a club drug, called K, Special K, Super K, and Vitamin K, among other names. Partiers inject it, put it in drinks, snort it, or add it to joints or cigarettes.
Dear colleagues in the Tennessee General Assembly, As you are called into special session to provide relief to Tennesseans still suffering from the hurricane last fall, you are being asked to once ...
FREDERICK, Md., Jan. 27, 2025 (GLOBE NEWSWIRE) -- Cartesian Therapeutics, Inc. (NASDAQ: RNAC) (the “Company”), a clinical-stage biotechnology company pioneering ...
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