...containing the Risk Evaluation and Mitigation Strategy (REMS) for its lead product ONSOLIS(TM) to the Food and Drug Administration (FDA) in December following a meeting with the FDA this week. In August 2008, BDSI received a Complete Response...
...icons link to social bookmarking sites where you can share this story and discover new Web pages. It took the U.S. Food and Drug Administration more than a century to grow into a massive, expensive, wasteful, inflexible, ineffective, distant and...
...as possible health risks. Most are ethnic treats, including snacks, drinks and chocolates. Itâs unusual for the Food and Drug Administration to put such a broad hold on goods from an entire country, not just a few rogue manufacturers. The order, which...
...mean we shouldn't keep monitoring to make sure things don't come up." SOURCES: Richard D'Amico, M.D., immediate past president, American Society of Plastic Surgeons; U.S. Food and Drug Administration; Nov. 18, 2008, Associated Press, Bloomberg...
Background
The Food and Drug Administration (FDA) is an agency of the United States Department of Health and Human Services and is responsible for the safety regulation of most types of foods, dietary supplements, drugs, vaccines, biological medical products, blood products, medical devices, radiation-emitting devices, veterinary products, and cosmetics. The FDA also enforces section 361 of the Public Health Service Act and the associated regulations, including sanitation requirements on interstate travel as well as specific rules for control of disease on products ranging from pet turtles to semen donations for assisted reproductive medicine techniques.
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Timeline
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Shao Mingli said this in:
14 hours ago from People's Daily Online