The Phase 1 clinical study of FAP-Exd (AVA6103) is anticipated to begin later in Q1 2026LONDON and PHILADELPHIA, (GLOBE NEWSWIRE) ...
The recall was issued last year when a supplier found a defect on some cans with easy-open pull tabs that compromised the ...
4don MSN
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 ...
A dietary supplement recall that sickened dozens of people across the United States has been expanded to Puerto Rico, Guam, the Virgin Islands and the United Kingdom.
Questions remain among top Food and Drug Administration officials over who has the appropriate legal authority to sign off on ...
Pharmaceutical company Boehringer Ingelheim said on Monday the U.S. Food and Drug Administration had approved its chewable ...
The U.S. Food and Drug Administration has delayed reviews of several drugs selected for the Trump administrations new ...
Conagra Brands added a "GLP-1 Friendly" label to 26 of its Healthy Choice frozen meals in early 2025. The Smoothie King chain ...
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.
Operating under the FDA's 503B pathway, the Apex facility will prioritize the production of generic shortage-listed ...
Some results have been hidden because they may be inaccessible to you
Show inaccessible results
Feedback