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Consumer web sites such as LivingSocial, Groupon, Loclly, and Ebates are popping up in millions of e-mail inboxes across the United States offering everything from sushi dinners and massages to car washes and now, healthcare.
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When review boards and research organizations' quality improvement (QI) offices work together, the net effect is a more thorough and efficient human subjects research process, experts say.
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The smartphone has helped drive the astronomical growth of the group coupon market, since notifications of daily coupons, also known as "daily deal alerts," are sent directly to the phone and the codes can be redeemed directly off of the device.
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In an updated report1 that appears in a recent issue of Journal of Palliative Medicine, researchers examined the ability to accessibility of palliative care in U.S. hospitals.
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IRBs and research offices need a variety of procedures and tools to ensure compliance. One tool that sometimes is overlooked is requiring research sites to develop corrective action plans (CAPs) when they have problems.
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Most major corporations and business sectors have adopted business quality improvement (QI) measures like Six Sigma, Lean Process, and others. But in human subjects research, this type of QI approach is fairly new, an expert says.
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In assessing the recent revisions to the Common Rule proposed by the Department of Health and Human Services (HHS), the accrediting agency for human subjects protection programs suggests that HHS may lack the necessary information to move forward with a final rule.
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Research ethicists and others have long described the value of recruiting more minorities in clinical research (CR) trials, but the question is whether or not IRBs have a role to play in advancing this goal.
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In the proposed revision of the Common Rule, the Department of Health and Human Services (HHS) responds to years of complaints about informed consent documents that they're too long, too complicated, too full of boilerplate and risk management language.
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When investigators seek an exception from informed consent (EFIC) for emergency research, they must show that they have engaged in community consultation and public disclosure, informing the public that they may encounter an experimental intervention while being treated in an emergency setting.
