Genentech Inc. won regulatory approval Tuesday to market an eye implant that can be refilled every six months with an already ...
Seven months after the FDA signed off on a reintroduction of Roche’s eye implant Susvimo, the U.S. regulator has broadened ...
Morgan Stanley analyst Erin Wright views the latest label change for Librela as “encouraging,” offering vets clarity in prescribing, and while ...
Open-label arm (infant participants < 1 year old) has been recently reviewed by a Data Monitoring Committee (DMC) and target drug ...
C&EN’s tabulation follows approvals from the FDA’s Center for Drug Evaluation and Research; therefore, it does not include blood products, gene therapies, vaccines, and other therapies that ...
The US Food and Drug Administration (FDA) is urging manufacturers to revise labeling of transmucosal buprenorphine products to ease access to higher doses needed due to the rise of high-potency ...
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The best way to check if a product has the dye is to read the label printed on the package. The FDA requires companies to disclose when they use color additives in their ingredients list.
with the EU requiring warning labels on products containing it. This isn't the first time the FDA has wielded the Delaney Clause—similar actions were taken against certain synthetic flavors in ...
File photo: US Sen. Richard Blumenthal responds to a question during a news conference at Hartford HealthCare on Jan. 2, 2025. Credit: Doug Hardy / CTNewsJunkie WASHINGTON – US Sen. Richard ...
a hit to his reputation and a decrease in his brand's value before his contract renegotiation with the record label this year. The suit added that UMG "understood the recording's inflammatory and ...
Food and Drug Administration officials granted a 2022 petition filed by two dozen food safety and health advocates, who urged the agency to revoke authorization for the substance that gives some ...