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(Reuters) – The U.S. Food and Drug Administration on Tuesday approved Japan-based Shionogi & Co Ltd’s treatment for low blood-platelet count or thrombocytopenia in patients with chronic liver disease. …
FDA Industry Systems (FIS) was created to facilitate making submissions to the U.S. Food and Drug Administration (FDA), including …
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The term “vaginal rejuvenation” has been thrown around for years, but what, exactly, it’s supposed to be is a little murky given that this isn’t an actual medical procedure. At its core, vaginal rejuv…
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A new Netflix documentary – The Bleeding Edge – highlights a wide range of systemic flaws in the FDA’s regulation of medical …
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Get to know FDA’s drug development and approval process — ensuring that drugs work and that the benefits outweigh their known risks. Guidance, Compliance & Regulatory Information Looking for FDA Guidance, Compliance, & Regulatory Information? Web page provides quick links to a variety of topics.
Endomag, the surgical guidance company, announced that it has received premarket approval (PMA) from the U.S. Food and Drug Administration (FDA) for Magtrace, the first non-radioactive, dual-tracer fo…
Home Page for the Food and Drug Administration (FDA)
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