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BioVex , a Woburn, Mass.-based biotechnology company that raised $40 million in venture capital in March to develop a novel cancer-fighting treatment, plans to announce Tuesday that it has raised another $30 million, The Boston Globe reported.
A drug industry group on Monday urged the U.S. Food and Drug Administration to adopt a universal safety symbol for Internet content containing FDA-approved information about a medicine or medical device.
( University of California - Los Angeles ) The drug Sprycel, approved for use by the US Food and Drug Administration in patients with chronic myeloid leukemia, significantly inhibited the growth and invasiveness of ovarian cancer cells and also promoted their death, a study by researchers with UCLA's Jonsson Comprehensive Cancer Center found.
No data in Celgene abstract, disappointing investors.
Glistening oysters cradled on beds of ice have provoked a political battle, with fishing industries along the Gulf Coast and their allies in Congress pitted against food safety officials in the Obama administration, who are determined to sanitize raw oysters.
Updated code is a model for state, city, county, tribal, territorial agencies and industry.
Worldwide deal involves privately held Alder BioTherapeutics
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Arena Pharmaceuticals Inc. on Tuesday posted a smaller third-quarter loss following completion of clinical testing of its obesity drug candidate lorcaserin.
With demand for the swine flu vaccine outpacing supply, the CDC says it's open to considering importing a generic flu drug from India. There's just one problem: The brand-name drug is still under U.S. patent. The company's chairman says he just wants to help.
"GMA" investigates spinach and leafy green safety standards.
The Food and Drug Administration needs three more months to review an application to a neuropathic pain drug being developed by XenoPort Inc. and GlaxoSmithKline PLC, the companies said.
Zacks Industry Outlook Highlights: Alcon, Novartis, Gilead Sciences, Biogen Idec and Acorda Therapeutics
WASHINGTON, Nov. 9 (UPI) -- The U.S. Food and Drug Administration says it has approved a new treatment for patients with a rare form of cancer known as Cutaneous T-cell Lymphoma.
WASHINGTON, Nov. 9 (UPI) -- The U.S. Food and Drug Administration says it has released an updated FDA Food Code that's used as a model for state, city, county and tribal inspections.
In consultation with the U.S. Food and Drug Administration (FDA), McNeil Consumer Healthcare, Division of McNEIL-PPC, Inc., is initiating a voluntary recall of a limited number of product lots of TYLENOL Arthritis Pain Caplet 100 count bottles, with the distinctive red EZ-OPEN CAP.
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