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As of Jan. 1, your accredited hospital was required to collect and report data on one additional core measure set as part of an expansion of the Joint Commission on Accreditation of Healthcare Organization's ORYX initiative.
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In light of changes to the survey process made last year, what does my ED need to provide to surveyors to demonstrate compliance with staffing effectiveness standards?
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The question remains: Is full-panel review necessary?
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IRB members who are confused about whether research containing an oral history is subject to IRB review are not alone. The Office for Human Research Protections (OHRP) has written two letters on the matter, leaving some room for contradictory interpretation until guidelines are issued, possibly this year.
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Small colleges and undergraduate departments at universities are finding it increasingly important to formalize their human subject protection programs while making certain IRBs are reviewing what they should and not filling agendas with a lot of unnecessary reviews, several experts say.
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Human subjects training is typically a part of human subjects protections programs. Such training has taken the form of in-house seminars given at regular intervals and web-based activities. Regardless of the form, the objectives are simple: Give those involved in human subject research ethics and regulatory information that will promote beneficence and compliance with regulations.
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In 1999, Chrissy Parker was a typical 14-year-old high school freshman riding home from school with a friend. Now, Parker is a college freshman whose name is frequently mentioned these days in the same sentence as Christopher Reeve.
