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FDA moves to curb Avastin's approval for breast cancerThe Food and Drug administration on Thursday revoked its approval of Roche drug Avastin for the treatment of breast cancer. The agency's action, based on findings that did not confirm that the medicin2010/12/21
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China Nuokang Bio-Pharmaceutical Provides Update on Dipyridamole Aspirin Receives Manufacturing License for Dipyridamole AspirinChina Nuokang Bio-Pharmaceutical Inc. (Nasdaq:NKBP) ("Nuokang" or the "Company"), a leading China-based biopharmaceutical company focused on the research, development, manufacture, marketing and sales2010/12/20
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European Medicines Agency recommends action plan to deal with possible presence of endotoxins in Baxter peritoneal dialysis solutionsThe European Medicines Agency has been informed by Baxter of the potential presence of endotoxins in their peritoneal dialysis solutions Dianeal, Extraneal and Nutrineal. These are sterile solutions u2010/12/20
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FDA Begins Process to Remove Breast Cancer Indication from Avastin LabelDrug not shown to be safe and effective in breast cancer patients ROCKVILLE, Md., Dec. 16, 2010--The U.S. Food and Drug Administration announced today that the agency is recommending removing the b2010/12/17
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BASF completes acquisition of CognisLudwigshafen, Germany – December 10, 2010 – BASF successfully completed its acquisition of Cognis Holding GmbH from Cognis Holding Luxembourg S.à r.l. controlled by Permira Funds, GS Capital Partners2010/12/17
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Illegal online drug sellers prey upon 36 million Americans~Research about Dangerous Practice – and the 11 Internet Commerce Companies Partnering Together to Protect Patients – Announced as Part of White House Forum~ Illegal online drug sellers have provid2010/12/16
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China Nuokang receives SFDA manufacturing license for Dipyridamole AspirinChina Nuokang Bio-Pharmaceutical Inc. (Nasdaq:NKBP) ("Nuokang" or the "Company"), a leading China-based biopharmaceutical company focused on the research, development, manufacture, marketing and sales2010/12/16
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GAO Report Faults FDA’s Response to Heparin CrisisAgency’s use of outside experts violated ethics rules Although the U.S. Food and Drug Administration’s (FDA) response to the contamination of heparin sodium in 2008 helped protect the public health,2010/12/15
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Bohai to acquire rights to 14 approved Traditional Chinese Medicines for $7,200,000Bohai Pharmaceuticals Group, Inc. (OTCBB/OTCQB: BOPH), a China-based pharmaceutical company engaged in the production, manufacturing and distribution of Traditional Chinese Medicine (TCM), has entered2010/12/15
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FDA warns consumers to avoid Man Up Now capsulesProduct marketed for sexual enhancement contains potentially dangerous ingredient The U.S. Food and Drug Administration is warning consumers not to use Man Up Now capsules, marketed as a dietary su2010/12/14