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While some publications have focused on the restriction of Propofol use by ED physicians and nurses under new rules issued in December 2009 by the Centers for Medicare and Medicaid Services (CMS), many observers say the issue is much larger, and that it deals with who can administer what ED providers consider procedural sedation and what CMS considers anesthesia.
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When a patient clicks on a link from the Web site of an organization such as KS&A to express an interest in participating in medical research, it sets off a chain of questions and choices that help that patient tailor the security to his or her own preferences.
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Each year the Council for Certification of IRB Professionals (CCIP) meet with representatives of the Professional Testing Corp. (PTC) to prepare the next year's Certified IRB Professional (CIP) examination.
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When a research network sets out to conduct multisite trials, IRBs can sometimes be seen as an obstacle that must be overcome.
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A project in Nashville, TN, to engage the community in cancer clinical trials has borne more fruit than its organizers had initially hoped.
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One of the chief benefits of installing an electronic IRB system is that it will automatize many of the standard administrative duties for IRBs and give managers and staff more time for work that will enhance human subjects protection.
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The Office for Human Research Protection (OHRP) has made educational videos available for the first time on the U.S. Department of Health and Human Services' YouTube channel.
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Trying to recruit people with medical conditions for research while maintaining their confidentiality can be a challenging task.
