What’s the Difference Between the FDA and the USDA?
Explaining America’s weirdly complicated food inspection system, including who regulates poultry and eggs and how Robert F. Kennedy Jr. is involved ...
U.S. News & World Report15d
US FDA Identifies Cybersecurity Risks in Certain Patient Monitors
(Reuters) - The U.S. Food and Drug Administration (FDA) said on Thursday it had identified three cybersecurity risks associated with certain patient monitors from Contec and Epsimed and urged ...
Toronto Star16d
FDA approves painkiller designed to eliminate the risk of addiction associated with opioids
WASHINGTON (AP) — Federal officials on Thursday approved a new type of pain pill designed to eliminate the risks of addiction and overdose associated with opioid medications like Vicodin and ...
al.com17d
Lay’s potato chip recall elevated to FDA’s highest-risk classification
The FDA has upgraded a recall of Lay’s Potato Chips to the highest level possible, meaning consuming the chips will cause adverse health consequences. In December, Texas-based food manufacturer ...
Medical Design and Outsourcing24d
Cortland Biomedical secures FDA registration
Cortland, New York – Cortland Biomedical, a full-service biomedical textile product development partner that provides access to a full spectrum of global engineering, design, and manufacturing ...
UPI24d
FDA approves Spravato, first monotherapy nasal spray to treat depression
the FDA announced Tuesday. Advertisement MDD is one of the most common psychiatric disorders, with an estimated 21 million adults in the United States living with the disease, according to Johnson ...
The Straits Times24d
US FDA approves standalone use of J&J’s ketamine-derived depression treatment
The US Food and Drug Administration (FDA) has expanded the approval for Johnson & Johnson’s nasal spray Spravato to allow its standalone use in patients with depression, the company said on Jan 21.
The Hill25d
Food companies want to confuse consumers. The FDA must push back.
The FDA recently submitted a proposed front-of-package labeling rule to the Office of Information and Regulatory Affairs. This proposed rule takes us one step closer to advancing a strong front-of ...
Reuters25d
US FDA puts clinical hold on Atara's trials for cancer cell therapies
While the FDA's decision prevents the company from enrolling ... from April 2:29 AM UTC · Updated ago category South32 sees US aluminium tariffs as negotiating tactic 2:28 AM UTC · Updated ...
JD Supra26d
FDA’s Catch-Up Plan on Cosmetics Faces Likely Regulatory Delays with Change in Administrations
FDA held a public listening session in June 2023 and opened a docket to receive written comments by July 2023 to satisfy this requirement. A significant number of public comments supported ...