Search for: "United States Food and Drug Administration" Results 21 - 40 of 6,111
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28 May 2024, 6:28 am by The Petrie-Flom Center Staff
Schedule 3 drugs must be approved by the Food and Drug Administration (FDA,) prescribed by a doctor, and distributed by a pharmacy. [read post]
27 May 2024, 10:00 pm by Sherica Celine
Counsel your healthcare organization clients on the Health Insurance Portability and Accountability Act (HIPAA), federal Common Rule, and Food and Drug Administration (FDA) regulations, which set the standards for maintaining the privacy and confidentiality of data obtained from participants in clinical trials. [read post]
27 May 2024, 9:05 pm by Katie Cohen
Although there are on average 2.7 patents per drug, a 2018 study found that each of the 12 top-selling drugs in the United States had on average 71 patents. [read post]
21 May 2024, 7:58 pm by Kurt R. Karst
  For OASH, the findings warranted a Food and Drug Administration (“FDA”) assessment under a second part to determin [read post]
21 May 2024, 1:38 pm by Laura Ray
Food and Drug Administration, HHS recommended to the DEA that marijuana be placed in Schedule III of the CSA. [read post]
20 May 2024, 10:00 pm by Sherica Celine
Read now » Related Content FDA Food and Dietary Supplements Regulatory Activity Tracker Monitor Food and Drug Administration (FDA) regulatory activity affecting food and dietary supplement companies. [read post]
19 May 2024, 9:05 pm by The Regulatory Review
Apr 10, 2023 | Solving State Transmission Roadblocks to Unlock Renewable Energy | Scholar examines how community-based regulatory reforms can support efforts to scale up the United States’ electric grid. [read post]
19 May 2024, 9:15 am by Gene Quinn
Senator Thom Tillis (R-NC) has been unsuccessfully trying to obtain information from the Food and Drug Administration (FDA) and the United States Patent and Trademark Office (USPTO) on data being used to support drug pricing proposals for nearly two and a half years. [read post]
19 May 2024, 9:15 am by Gene Quinn
Senator Thom Tillis (R-NC) has been unsuccessfully trying to obtain information from the Food and Drug Administration (FDA) and the United States Patent and Trademark Office (USPTO) on data being used to support drug pricing proposals for nearly two and a half years. [read post]
15 May 2024, 9:05 pm by Coral Beach
  “I urge the Food and Drug Administration to take similar action in response to these findings. [read post]
15 May 2024, 9:04 pm by Dan Flynn
Food and Drug Administration (FDFA) completed its pre-market evaluation of food made from cultured animal cells by GOOD Meat. [read post]
15 May 2024, 1:56 pm by kblocher@hslf.org
Food and Drug Administration’s regulations and guidance documents for pharmaceutical companies are unclear and continue to emphasize the use of animals for drug testing. [read post]
15 May 2024, 7:00 am by Yosi Yahoudai
Deaths from drug overdoses fell last year in the United States as fewer people lost their lives to fentanyl and other opioids, marking the first time the death toll had dropped in five years, according to newly released estimates from the Centers for Disease Control and Prevention. [read post]
15 May 2024, 4:29 am by Yosi Yahoudai
In the United States, the rate in Black women is about 60% higher than in White women. [read post]
15 May 2024, 2:33 am by kblocher@hslf.org
The Humane Society of the United States and Humane Society Legislative Fund petition FDA to revise outdated drug testing regulations kblocher@hslf.org Wed, 05/15/2024 - 09:33 WASHINGTON (May 15, 2024)—Today, the Humane Society of the United States and Humane Society Legislative Fund filed a petition with the Food and Drug Administration requesting that the agency updates regulations to make clear that animal… [read post]
14 May 2024, 9:06 pm by Coral Beach
Food and Drug Administration has approved various foods for irradiation, including meat, poultry, fresh shell eggs, and spices. [read post]
14 May 2024, 9:05 pm by Dan Flynn
  Food and Drug Administration (FDA) defines a product for personal importation as not for further sale or distribution into U.S. commerce. [read post]
7 May 2024, 2:00 am by Moll Law Group
  The United States Food and Drug Administration has informed doctors, nurses and other health care providers that it is imposing new labeling updates for Becton, Dickinson and Company mesh products. [read post]
5 May 2024, 9:03 pm by News Desk
Food and Drug Administration for violations in their production facility. [read post]