After winning a breakthrough therapy designation for its Hunter syndrome enzyme replacement therapy, Denali Therapeutics is ...
Genentech Inc. won regulatory approval Tuesday to market an eye implant that can be refilled every six months with an already ...
Drug discovery is the process through which potential new medicines are identified. It involves a wide range of scientific disciplines, including biology, chemistry and pharmacology. Large-scale ...
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 ...
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 ...