EEG was essential in assessing the drug’s ketamine-like antidepressant effects on the brain. The second paper, entitled "Evaluating an EEG-based tool for assessing acute clinical and cognitive changes ...

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 ...

On his first day in office, President Donald Trump designated drug cartels as terrorist organizations. The executive order fuses the “war on drugs” with the “war on terror,” expanding the legal tools ...

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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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 ...

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The National Fisheries Institute (NFI) and other organizations are concerned about new front-of-package (FOP) nutrition labels the U.S. Food and Drug Administration (FDA) is proposing for most ...

On Wednesday, the Food and Drug Administration (FDA) proscribed the dye based on a 2022 petition by consumer advocacy groups against its use, which had already been banned in cosmetics 35 years ago.