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The past decade has seen malaria control return to the forefront of global public health agendas.
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In this issue: Antiviral drugs and birth defects, bisphosphonates and esophageal cancer, naltrexone plus bupropion for weight loss, 2010-11 influenza vaccine, FDA Actions.
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The first step in improving a clinical trial site's good clinical practice is to make certain all informed consent processes and documentation are followed with exacting care.
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Most work environments contain at least one example of clashing personalities or a problematic worker attitude.
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Research institutions continually look for ways to make their operations more efficient, especially during lean economic times.
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Often overshadowed by other pressing clinical research needs, the detailed, difficult process of data management is drawing closer scrutiny by the Food and Drug Administration, researchers are finding.
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Clinical trial data increasingly is collected and communicated electronically. Sites often are dependent on how sponsors and clinical research monitoring organizations set up their data collection and editing systems, but there are issues they can prevent through better processes and preparation.
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In clinical research documentation, the little things definitely count and often could lead to major regulatory problems.
