The FDA encourages sponsors to discuss plans to use animal testing alternatives, called new approach methodologies or NAMs, ...
On , The US Food and Drug Administration issued draft guidance identifying specific types of monoclonal antibody products for which the agency believes six-month toxicity testing in non-human primates ...
The Physicians Committee for Responsible Medicine applauds the Food and Drug Administration’s newly released draft guidance, ...
Dec 2 (Reuters) - The U.S. Food and Drug Administration on Tuesday issued new draft guidance on reducing the use of lab ...
The Well News on MSN
FDA Draft Guidance Places New Limits on Toxicity Tests Involving Primates
WASHINGTON - The Food and Drug Administration released a draft guidance on Tuesday significantly reducing the range of ...
Pharmaceutical Technology on MSN
FDA steps back from preclinical primate testing amid wider regulatory shift
New non-primate draft guidance follows the agency’s wider aim to curtail the use of animal testing in preclinical toxicology.
The draft guidance issued Tuesday comes as regulators and policymakers have looked for ways to aid U.S. drugmakers amid fast progress by their China-based counterparts.
The new law will allow the state to publish guidelines that differ from the CDC.
FOX 5 Atlanta on MSN
FDA plans stricter vaccine approval rules
The FDA plans to impose stricter vaccine approval rules, prompting warnings from Georgia doctors who fear the policy could ...
"We have relied on this federal system for trusted medical guidance in 1930. And it's been eviscerated. The trust is gone." ...
New guidelines from the World Health Organization (WHO) recommend using GLP-1 medications to help manage obesity along with a ...
As many as 1 in 4 breast cancers occur in women younger than 50, researchers said at the Radiological Society of North ...
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