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U S Food and Drug Administration Home Page
Home Page for the Food and Drug Administration (FDA)
Food and Drug Administration - Wikipedia, the free encyclopedia
The Food and Drug Administration (FDA or USFDA) is an agency of the United States Department of Health and Human Services, one of the United States federal executive ...
Drugs - U S Food and Drug Administration Home Page
Same quality standards; FDA approved ; Infographic outlines what you need to know; Facts about Generic Drugs; Narratives from clinical science experts
FDA.COM Information Portal
FDA.COM Food and Drug Assistance - Resources for the Food, Drug and Device Industry - Advertise 856-810-1825
Foods - U S Food and Drug Administration Home Page
consumer@fda.gov. Industry: industry@fda.gov. Center for Food Safety and Applied Nutrition. Food and Drug Administration. 5100 Paint Branch Parkway. College Park, MD ...
Recalls, Market Withdrawals, & Safety Alerts
FDA works with industry and our state partners to publish press releases and other public notices about recalls that may potentially present a significant or serious ...
Center For Health and Wellness; FDA Regulations, FDA Compliance ...
Resources for Health, Wellness, FDA Regulations, FDA Compliance, Clinical Trials, FDA Recalls and 21 CFR Part 11 Compliance.
Drugs@FDA: FDA Approved Drug Products - U S Food and Drug ...
A searchable catalog of FDA approved drug products both prescription and over the counter. The database includes information such as therapeutic equivalents and links ...
FDA Sheds Light on Sunscreens - U S Food and Drug Administration ...
FDA is enacting new regulations for testing and labeling of sunscreens to provide consumers with the information they need to choose a sunscreen product that provides ...
US FDA Industry Systems
FDA Industry Systems (FIS) was created to facilitate making submissions to the U.S. Food and Drug Administration (FDA), including registrations, listings, and other ...

News Results

FDA to scrutinize safety of metal-on-metal hip implants
(AP) WASHINGTON -- Metal hip replacements implanted in a half-million Americans may be failing earlier than expected, but it could be years before U.S. health regulators have a clear picture of the scope of the problem. The Food and Drug ...
CBS News
UPDATE 2-US FDA rebuffs Bristol/Pfizer clot preventer
June 25 (Reuters) - A closely watched blood clot preventer from Bristol-Myers Squibb Co and Pfizer Inc failed to win approval from U.S. health regulators, the companies said on Monday, sending their shares lower. Shares of Bristol fell nearly 4 ...
FDA Says No to Pfizer, Bristol Anti-Clotting Drug
The FDA rejects, at least for now, the new anti-clotting drug from Bristol-Myers and Pfizer. According to the companies, the agency is requesting “additional information on data management and verification” from the key trial that raised ...
Wall Street Journal
FDA accuses Amylin of withholding info
A top US regulator has accused Amylin, the biotech company, of withholding important information on cardiac side effects of its drugs, casting a shadow over competitive bidding for the business by several large pharmaceutical groups. In a ...
Financial Times
The Clot Thickens: FDA Delays The Pfizer And Bristol-Myers Bloodthinner, Again
Once again, the FDA has delayed approval for the widely anticipated Eliquis bloodthinner. In a move that surprised investors, the agency issued a so-called complete response letter to Pfizer and Bristol-Myers Squibb, which hoped to begin ...
Dynavax Announces FDA Acceptance of HEPLISAV(TM) BLA
Dynavax Technologies Corporation (NASDAQ: DVAX) today announced that the Food and Drug Administration (FDA) has accepted for review the U.S. Biologics License Application (BLA) for HEPLISAV, pursuing an indication for immunization against infection caused ...
FDA: Stem cell lab used by Perry has problems
HOUSTON (AP) — The U.S. Food and Drug Administration has issued a new report criticizing the Texas company that stored adult stem cells from Texas Gov. Rick Perry for use in an experimental procedure for his back pain, according to a newspaper report Monday.
Eye To Eye: FDA Approves First Glaucoma Stent For Use With Cataract Surgery
(RTTNews) - iStent, the smallest medical device ever implanted into the human body, developed by ophthalmic medical device company Glaukos Corp., was approved by the FDA on Monday for use in combination with cataract surgery for the treatment of open-angle ...
RTT News
FDA bill no model for bipartisanship
The bipartisan treatment the FDA user fee bill has enjoyed did not fall like manna from heaven. It came at the insistence of the pharmaceutical and medical device industries, the FDA and legislators on both sides of the aisle who agreed early on ...
FDA Wants More Apixaban Data
The FDA said Monday that it needs more data before it can approve apixaban, an oral factor Xa inhibitor, for prevention of stroke in patients with nonvalvular atrial fibrillation. The drug is approved and marketed in Europe under the trade name ...
MedPage Today
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