The Food and Drug Administration put patients' lives at risk by halting enforcement of 30-year-old requirements that medical device makers meet federal laboratory standards prior to testing their products on humans, a watchdog group charges in a new report.
The rules at issue cover studies on an array of devices, including life-saving products such as defibrillators, pacemakers, coronary stents and heart valves.
Bush FDA decision put patients in danger
Donald Trump announced a new package of tariffs on Tuesday, this time on generic drugs made...
One of the strictest abortion bans in the country will be on the ballot this November...
One in four Israelis now engages in harmful substance use as the psychological fallout from Israel’s...
