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Exclusive: US FDA delays two drug reviews in new voucher program after safety, efficacy ...
The U.S. Food and Drug Administration has delayed reviews of two drugs chosen for the Trump administration's new fast-track ...
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Legal questions swirl around FDA's new expedited drug program, including who should sign off
A plan to slash Food and Drug Administration drug review times is raising alarms at the public health agency that's been ...
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Takeaways from the AP's report on turmoil surrounding the FDA's new fast-track drug program
A plan to slash drug review times at the Food and Drug Administration is sparking deep concerns among agency staffers and ...
LOS ANGELES (KABC) -- The Food and Drug Administration's approval process is one of the most stringent in the world, but now some experts are questioning newer drugs that go through a quicker review.
In early 2025, the FDA was rocked by sweeping layoffs and leadership turnover, raising questions about whether the agency ...
The FDA has delayed reviews of two drugs in the Trump administration's fast-track program due to safety concerns, including a ...
The Food and Drug Administration (FDA) development and approval process for drugs and medical devices involves multiple phases that ensure the safety and effectiveness of products before and after ...
An FDA draft guidance nixing the requirement for biosimilar manufacturers to conduct comparative efficacy studies may prove ...
Each year, the FDA approves a wide range of medications that help shape the future of medicine in the U.S. These include novel drugs that offer new treatment options, as well as first generics and ...
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Drugmakers told the FDA that inflexible post-approval change requirements are among the top regulatory barriers to the ...
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