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Legal questions swirl around FDA’s new expedited drug program, including who should sign off
A plan to slash Food and Drug Administration drug review times is raising alarms at the public health agency that's been ...
Pharmaceutical company Boehringer Ingelheim said on Monday the U.S. Food and Drug Administration had approved its chewable ...
Questions remain among top Food and Drug Administration officials over who has the appropriate legal authority to sign off on ...
The U.S. Food and Drug Administration has delayed reviews of several drugs selected for the Trump administrations new ...
The U.S. Food and Drug Administration (FDA) has granted full approval of Laverdia, a drug to treat dogs with lymphoma, a type ...
A new study published in Therapeutic Innovation & Regulatory Science provides crucial insights into the design and ...
Some major drugmakers are hesitating to participate in the Trump administration's speedier review program for new medicines ...
An Instagram ad catches your eye. You click to the product’s website and find reassurance: The product, it says, is "FDA certified" or was "produced in an FDA registered facility." Mention of the U.S.
Friendly” labels on the packaging are becoming more common in U.S. supermarkets as a growing number of Americans try obesity ...
— Novel, third-generation PCSK9 inhibitor designed to help patients more easily achieve lifelong cholesterol goals with robust and sustained LDL-C reductions of 50% or more — — Approved for adults ...
Inquirer.net on MSN
FDA: Lack of food safety limits not a 'shield against accountability'
The Food and Drug Administration (FDA) on Tuesday warned manufacturers that the lack of specific safety limits cannot be used ...
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