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Cell Genesys, Inc. (Nasdaq:CEGE) announced that it has terminated VITAL-2, the second of two Phase 3 clinical trials of GVAX immunotherapy for prostate cancer, which compares GVAX immunotherapy in combination with Taxotere® (docetaxel) to Taxotere
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American Bio Medica Corporation (NASDAQ:ABMC) announced that the US Food and Drug Administration (FDA) has granted CLIA waived status to the Company's Rapid TOX® point of collection drug test product line. The waiver applies to all 14 drugs that the
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Elekta recently announced that it has received CE Mark clearance to distribute Elekta Compact(TM), the latest addition to its line of treatment systems, offering clinicians an easy to implement, more affordable solution for radiation the
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Amylin Pharmaceuticals, Inc. (Nasdaq: AMLN) and Eli Lilly and Company (NYSE: LLY) in a conference call today provided context and additional information regarding the August 18, 2008 U.S. Food and Drug Administration (FDA) update to a p
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The key points from the latest release are: Performance on the five standards has remained around their highest recorded levels, during the period April to June 2008, namely: - 99.9% of patients were seen within 2 weeks from urgen
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The General Optical Council (GOC) has been praised by the Council for Healthcare Regulatory Excellence (CHRE) for successfully meeting the required standards of performance in all aspects of its work. In its annual Performance Assessment of how th
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While jams and other consumer products are strictly regulated and are required to pass stringent tests before they can be sold, tobacco has no restrictions and manufacturers can, and do, add anything they want into the product.
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This is the fourth quarterly practice survey, covering a sample of practices from each primary care trust (PCT), conducted between June and August 2008. The aims of the survey are to get feedback from practices on their perception of th
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