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A recent controversial move by a federal health agency to shut down a highly successful infection prevention program because it appeared to be involved in human research rather than quality improvement has ominous implications for traditional infection control activities, a leading epidemiologist tells Hospital Infection Control.
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The Centers for Disease Control and Prevention in conjunction with Kaiser Permanente's Northern California Division of Research will formally investigate an unexplained but persistently reported skin condition known as Morgellons.
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Clinical trial investigators and sites increasingly may need to rely on recruitment experts in coming years as community-based research increases and the industry evolves.
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The informed consent process is more challenging because of the public's lack of understanding and trust of research.
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Clinical research professionals at Summa Health System in Akron, OH, have found that some details on recruitment materials can make a big difference in how potential research participants view a clinical trial.
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Clinical trial sites and research professionals should be cautious and learn from their peers' mistakes to prevent clinical research (CR) litigation, experts say.
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Clinical research teams and investigators may find that their traditional strategies for handling incidental findings during a trial are inadequate in this age of genetic research.
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Investigators too often use informed consent documents that lack the simple language and optimal reading level for communicating information to potential volunteers, an expert says.
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This single-center, retrospective study examined ICU mortality and various risk factors among critically ill patients who developed bacteremia during their VAP episode.
