Search for: "FOOD AND DRUG ADMINISTRATION"
Results 2041 - 2060
of 23,781
Sort by Relevance
|
Sort by Date
27 Jan 2023, 5:16 am
She was simply quoting a comical interaction between Molly Jong-Fast and her husband, who was about to take food away from her. [read post]
26 Jan 2023, 9:06 pm
Pulling from the panel’s recommendations, the Food and Drug Administration’s path to a safer food supply seems clear albeit a lot to chew on: Most FDA employees understand the immense responsibility of the Agency’s Human Foods Program, appreciate the importance of their work, and share a common value of striving to protect public health. [read post]
26 Jan 2023, 9:03 pm
Food and Drug Administration (FDA) proposed new guidelines for maximum lead limits in baby food. [read post]
26 Jan 2023, 6:49 pm
Food and Drug Administration convened a high-level internal working group to... [read post]
26 Jan 2023, 2:06 pm
Food and Drug Administration (FDA) is working with Congress to develop a new regulatory framework for cannabidiol (CBD) products. [read post]
26 Jan 2023, 12:51 pm
Buried in the “Miscellaneous” chapter of Subtitle F (“Cross-Cutting Provisions”) of the Food and Drug Administration Title (Title III) of the 2023 CAA is Section 3630, a provision without a short title called “Facilitating exchange of product information prior to approval. [read post]
26 Jan 2023, 12:04 pm
The Food and Drug Administration said there are too many unknowns about CBD products to regulate them as foods or supplements under the agency’s current structure. [read post]
26 Jan 2023, 9:15 am
Food and Drug Administration (FDA) to treat melanoma, renal cell carcinoma, colorectal cancer, hepatocellular carcinoma, non-small cell lung cancer (NSCLC), malignant pleural mesothelioma, and esophageal cancer, either alone or in combination with the company's drug, Opdivo. [read post]
26 Jan 2023, 9:15 am
Food and Drug Administration (FDA) to treat melanoma, renal cell carcinoma, colorectal cancer, hepatocellular carcinoma, non-small cell lung cancer (NSCLC), malignant pleural mesothelioma, and esophageal cancer, either alone or in combination with the company's drug, Opdivo. [read post]
25 Jan 2023, 8:30 pm
Mifepristone is a generic medication abortion pill approved by the US Food and Drug Administration (FDA) to be used up to ten weeks of pregnancy. [read post]
25 Jan 2023, 8:23 pm
As the Federal Food, Drug and Cosmetic Act (FDCA) allows the Food and Drug Administration (FDA) to regulate medication, Bryant contends that additional restrictions imposed on the prescription of mifepristone by North Carolina are in conflict with the FDCA. [read post]
25 Jan 2023, 1:33 pm
Food and Drug Administration that he will be resigning his position as Deputy Commissioner for the Office of Food Policy and Response at the FDA effective Feb. 24. [read post]
24 Jan 2023, 9:05 pm
Food and Drug Administration Tuesday announced draft guidance for the industry on “action levels” for lead in processed foods that are intended for babies and children under two years old, for the purpose of reducing potential health effects in this vulnerable population from dietary exposure to lead. [read post]
24 Jan 2023, 5:34 pm
Food and Drug Administration also conducted an investigation and on Dec. 9, 2022, sent a warning letter to Big Olaf. [read post]
24 Jan 2023, 5:22 pm
Food and Drug Administration (FDA) 483 report Philips knew about the foam and the issues with it since at least 2015. [read post]
23 Jan 2023, 10:00 pm
Among other things, the court didn’t find the labeling deceptive, and cited to information publicly posted on the Food & Drug Administration’s website which unequivocally reflects that juices are commonly pasteurized or otherwise treated to kill potentially harmful bacteria. [read post]
23 Jan 2023, 9:01 pm
The Food and Drug Administration is continuing its use of import alerts to enforce U.S. food safety regulations for food from foreign countries. [read post]
23 Jan 2023, 9:00 pm
Food and Drug Administration (FDA), and this workshop will do just that. [read post]
23 Jan 2023, 6:55 pm
Livornese —Last month, Congress took a big step towards improving clinical trial diversity by requiring sponsors of most drug and device clinical studies to submit a diversity action plan when they submit key trial documents to the Food and Drug Administration (FDA). [read post]
23 Jan 2023, 4:15 am
Aug. 5, 2022) -- affirming district court’s decision that Exemption 4 protected portions of pharmaceutical company's successful application for accelerated approval of a drug. [read post]
