Search for: "UNITED STATES FOOD AND DRUG ADMINISTRATION" Results 581 - 600 of 6,146
Sort by Relevance | Sort by Date
RSS Subscribe: 20 results | 100 results
28 Dec 2022, 11:42 am by kblocher@hslf.org
As the year was coming to an end, as part of a U.S. federal spending bill, we secured $5 million within Food and Drug Administration’s budget specifically for nonanimal methods. [read post]
27 Dec 2022, 9:05 pm by Series of Essays
The Regulatory Challenges of FinTech June 14, 2022 | Jillian Moss Scholar sketches the current regulatory landscape for financial technologies in the United States. [read post]
24 Dec 2022, 6:50 pm by Bill Marler
According to the CDC, it is estimated that 1.4 million cases of salmonellosis occur each year in the United States. [read post]
24 Dec 2022, 8:45 am by Holman
  In 2004, the United States Food and Drug Administration (“FDA”) granted pirfenidone orphan drug status for treatment of patients with idiopathic pulmonary fibrosis (“IPF”), a chronic, irreversible lung disease. [read post]
24 Dec 2022, 8:10 am by Joel R. Brandes
It observed that pursuant to Family Court Act § 1046(a)(iii), “proof that a person repeatedly misuses a drug,” under certain circumstances, constitutes “prima facie evidence that a child of ... such person is a neglected child. [read post]
23 Dec 2022, 9:06 pm by Dan Flynn
NAUGHTY — The “F” in Food and Drug Administration was as bad as it gets this year. [read post]
23 Dec 2022, 8:27 am by kblocher@hslf.org
Finally, the omnibus includes the full President’s budget request of $5 million for the Food and Drug Administration to develop and implement new approach methodologies to replace animal testing. [read post]
22 Dec 2022, 9:07 pm by Elizabeth Penava
Food and Drug Administration approval, they still cannot be legally prescribed because of their status as Schedule I substances, Lamkin contended. [read post]
22 Dec 2022, 6:31 am by Ben Vernia
Such other devices may include telephones, alarm and security systems, televisions and radios.The settlement resolves allegations that Advanced Bionics, in submitting pre-market approval applications to the Food and Drug Administration (FDA) for Advanced Bionics’ Neptune and Naida cochlear implant processors, made false claims regarding the results of its RF emissions tests. [read post]
20 Dec 2022, 1:52 pm by kblocher@hslf.org
Finally, the omnibus includes the full President’s budget request of $5 million for the Food and Drug Administration to develop and implement new approach methodologies to replace animal testing. [read post]
20 Dec 2022, 5:00 am by Matthew Chun
Food and Drug Administration (FDA), which “regulates the sale of medical device products (including diagnostic tests) in the U.S. and monitors the safety of all regulated medical products. [read post]
17 Dec 2022, 12:53 pm by Bill Marler
Food and Drug Administration (FDA), the Texas Department of State Health Services, along with other state and local officials to investigate a multistate norovirus outbreak linked to raw oysters from harvest area TX 1, Galveston Bay, Texas. [read post]
16 Dec 2022, 9:04 pm by Madeline Bruning
Food and Drug Administration (FDA) serves as the primary regulatory body for medical device cybersecurity. [read post]
15 Dec 2022, 9:04 pm by Coral Beach
Food and Drug Administration (FDA) and public health officials from several states have been collecting samples of enoki mushrooms and found Listeria in many samples, resulting in more than 20 recalls of enoki mushrooms. [read post]
15 Dec 2022, 4:36 pm by Patti Waller
Food and Drug Administration (FDA), the Texas Department of State Health Services, along with other state and local officials to investigate a multistate norovirus outbreak linked to raw oysters from harvest area TX 1, Galveston Bay, Texas. [read post]
15 Dec 2022, 8:05 am by kblocher@hslf.org
Moreover, American horses routinely receive a wide array of medications and treatments that are expressly prohibited by the Food and Drug Administration for use at any time during the life of animals slaughtered for human consumption due to their toxicity to humans. [read post]
14 Dec 2022, 9:05 pm by Nicoletta Rangone
Food and Drug Administration uses post-market surveillance techniques to update rules and guidance. [read post]
14 Dec 2022, 4:15 am by Eileen McDermott
he United States Patent and Trademark Office (USPTO) sent out a reminder today to those interested in speaking at an upcoming Public Listening Session on collaboration efforts between the USPTO and Food and Drug Administration (FDA) that they must sign up to participate by January 5, 2023. [read post]
14 Dec 2022, 4:15 am by Eileen McDermott
he United States Patent and Trademark Office (USPTO) sent out a reminder today to those interested in speaking at an upcoming Public Listening Session on collaboration efforts between the USPTO and Food and Drug Administration (FDA) that they must sign up to participate by January 5, 2023. [read post]