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20 Dec 2016, 9:30 pm by Mariano-Florentino Cuéllar
Food and Drug Administration are just a few of the agencies turning to automation as a way to improve regulatory functioning. [read post]
20 Dec 2016, 1:59 pm by Steven Boutwell
Before Naloxone or other opioid antagonist drug product can be released to the recipient, the pharmacist shall verify the recipient’s knowledge and understanding of the proper use of the drug product including: (1) techniques on how to recognize signs of opioid-related drug overdose; (2) standards and procedures for the storage and administration of the drug product; and (3) emergency follow-up procedure including the requirement to summon emergency… [read post]
20 Dec 2016, 8:42 am by Associates and Bruce L. Scheiner
Food & Drug Administration’s 510(k) program, which allows drugs and medical products to be fast-tracked through the rigorous approval process if they are “substantially similar” to an item already on the market. [read post]
20 Dec 2016, 5:00 am by blackfin
They may be promoted by a government oversight agency, such as the Food and Drug Administration (FDA) or the Consumer Product Safety Commission (CPSC). [read post]
20 Dec 2016, 5:00 am by blackfin
They may be promoted by a government oversight agency, such as the Food and Drug Administration (FDA) or the Consumer Product Safety Commission (CPSC). [read post]
20 Dec 2016, 5:00 am by blackfin
They may be promoted by a government oversight agency, such as the Food and Drug Administration (FDA) or the Consumer Product Safety Commission (CPSC). [read post]
20 Dec 2016, 5:00 am by blackfin
They may be promoted by a government oversight agency, such as the Food and Drug Administration (FDA) or the Consumer Product Safety Commission (CPSC). [read post]
20 Dec 2016, 5:00 am by blackfin
They may be promoted by a government oversight agency, such as the Food and Drug Administration (FDA) or the Consumer Product Safety Commission (CPSC). [read post]
20 Dec 2016, 5:00 am by blackfin
They may be promoted by a government oversight agency, such as the Food and Drug Administration (FDA) or the Consumer Product Safety Commission (CPSC). [read post]
19 Dec 2016, 10:01 pm by Coral Beach
That brilliance will no doubt be eclipsed when the multi-national company begins marketing its genetically engineered, pink-fleshed version of the fruit with the tagline “extra sweet pink flesh pineapple” — as approved by the Food and Drug Administration. [read post]
19 Dec 2016, 10:00 pm by News Desk
“The Food and Drug Administration has been made aware of this recall,” according to the Snyder recall notice. [read post]
19 Dec 2016, 9:30 pm by Mariano-Florentino Cuéllar
Food and Drug Administration (FDA) often considers “Population Pharmacokinetics” models, which test how drugs will interact with different bodies, depending on age, weight, and other factors. [read post]
The Food and Drug Administration (“FDA”) released its final guidance on medical device safety on December 14, 2016, titled “Public Notification of Emerging Postmarket Medical Device Signals (Emerging Signals). [read post]
18 Dec 2016, 10:00 pm by News Desk
A dairy operation in Illinois and a seafood processor in Hawaii were on the receiving end of warning letters from the Food and Drug Administration according to the agency’s most recently published records. [read post]
18 Dec 2016, 9:30 pm by Mariano-Florentino Cuéllar
Think about the subtle choices involving drug approval, asylum applications, bioethics, and the protection of endangered species. [read post]
18 Dec 2016, 9:29 pm by RegBlog
Food and Drug Administration, for example, are starting to use complex computer models that can predict environmental exposure to chemicals and drug interactions across patient groups. [read post]
18 Dec 2016, 5:15 pm by Bruce Clark
Food and Drug Administration announced in Late November that the U.S. [read post]
17 Dec 2016, 10:00 pm by News Desk
Although no pathogenic bacteria have been found in the powdered milk product supplied in Williams-Sonoma’s product, we have decided out of an abundance of caution to recall the product produced from the specific lot received from our ingredient supplier,” according to the recall notice posted on the Food and Drug Administration’s website. [read post]