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By calling an 800 number and paying a $5 fee, residents in four Wyoming cities can have face-to-face consultations with clinical pharmacists, who not only review the residents health and medication history but make cost-saving suggestions as well.
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All AEs will be assessed by the investigator using the protocol-defined grading system. If the protocol has no defined grading system, or if the AE is not described in the existing grading system, the following guidelines should be used to qualify severity.
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No investigator or coordinator wants to believe it could happen. But in clinical trials, injuries or adverse events are always a possibility. The question for many is, What will happen to study subjects who are injured in the course of their research participation?
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The recent lawsuit against Abiomed Inc. of Danvers, MA, and others involved in clinical trials involving the AbioCor Implantable Replacement Heart shows that sometimes the best preparation and informed consent process still cannot prevent litigation.
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Director Argues for Rigorous CAM Research; WHO Issues Guidelines About Medicinal Plant Production and Collection; One-third of CAM Centers Have No Physician Involvement. Altern Ther Women's Health 2004;6(3):23-24.
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O'Mathuna DP. Therapeutic touch for pain. Altern Ther Women's Health 2004;6(3):17-20.
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In our cover story in the November 2003 issue, Tania Bridgeman, RN, PhD, director of clinical path development of the University of California at Irvine Medical Center, was quoted as using a clinical documentation system called TDF from Atlanta-based Eclypisis.
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U.S. Department of Health and Human Services (HHS) Secretary Tommy G. Thompson has released two reports that represent the first national, comprehensive effort to measure the quality of health care in America and differences in access to health care services for priority populations.
