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Training courses for the Undergraduate Medical Admissions Test (UMAT) are expensive, inequitable and don't improve students' chances of getting into medicine, according to the Australian Medical Students' Association (AMSA).
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Vitrolife has received approval from the Canadian authorities to start a study with STEEN Solution™. The study, which has been designed in consultation with the American FDA, is planned for quarters three to four of 2008 and will be the key element
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Researchers running cancer trials are often critical of the Research Ethics Committee (REC) process they have to go through to get their trials approved, complaining that it's too complex, burdensome and sometimes unreasonable. In the UK only 17% of
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According to a new Life Science Intelligence (LSI) Report, 2008 U.S. Markets for Spinal Disc Repair and Replacement Technologies , the U.S. market for artificial disc replacement will grow from $55 million in 2007 to $440 million by 2013. To date,
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Curis, Inc. (NASDAQ: CRIS), a drug development company focused on developing next generation proprietary targeted medicines for cancer treatment, announced the publication of preclinical data in Nature that support the premise that Hedgehog proteins
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Biogen Idec announced that enrollment is complete in the ASSURANCE trial, a long-term follow-up study which will assess up to 15 years of AVONEX® (interferon beta-1a) treatment in an effort to provide detailed data on the long term efficacy of the d
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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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