Practical tips for working effectively with your institutional review board.
The federal government regulates human research with a local institutional review board (IRB) at your institution. Your IRB's main responsibility is to protect the rights and welfare of human subjects recruited to participate in research. The IRB is responsible for reviewing and approving all resear...
| Publicado en: | Respiratory Care Vol. 53; no. 10; pp. 1354 - 1362 |
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| Autor principal: | |
| Formato: | tables/charts Journal Article |
| Publicado: |
Mary Ann Liebert, Inc.
Oct2008
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| Acceso en línea: | Ver este registro en EBSCOhost |
| fields | @attributes: recordID: 1 pdfLink: plink: https://search.ebscohost.com/login.aspx?direct=true&db=ccm&AN=105568237&site=ehost-live header: @attributes: shortDbName: ccm uiTerm: 105568237 longDbName: CINAHL Complete uiTag: AN controlInfo: bkinfo: dissinfo: jinfo: jid: 00201324 4GG jtl: Respiratory Care issn: 00201324 maglogo: N pubinfo: dt: Oct2008 vid: 53 iid: 10 pid: 1365 pub: Mary Ann Liebert, Inc. place: New Rochelle, New York artinfo: ui: 105568237 105568237 2010090650 NLM18812000 105568237 ppf: 1354 ppct: 8 formats: fmt: @attributes: type: P tig: atl: Practical tips for working effectively with your institutional review board. aug: au: Schwenzer KJ affil: Department of Anesthesiology, University of Virginia Health System, Charlottesville, Virginia sug: subj: Clinical Research Institutional Review Protection of Human Subjects Study Design Acronyms Conflict of Interest Consent (Research) Data Management Government Regulations Health Insurance Portability and Accountability Act Privacy and Confidentiality ab: The federal government regulates human research with a local institutional review board (IRB) at your institution. Your IRB's main responsibility is to protect the rights and welfare of human subjects recruited to participate in research. The IRB is responsible for reviewing and approving all research protocols that involve human subjects. The IRB evaluates your study design to ensure that it has the possibility of answering your research hypothesis. The IRB focuses on the risks and benefits of your research. The IRB wants to know that research subjects are recruited fairly and that the potential for benefit is distributed equitably. They also want to know how you plan to protect research subjects from the risks of research and how you will manage the data, especially protected health information. though the Code of Federal Regulations is extensive, this article provides information to help you navigate your research protocol through the layers of regulations, including the Privacy Rule of the Health Insurance Portability and Accountability Act of 1996. Whether conducting a simple chart review or participating in a multi-site randomized placebo-controlled trial, if you follow tried-and-true scientific methods and good clinical practice, you will be able to work effectively with your IRB. pubtype: Academic Journal doctype: tables/charts Journal Article ougenre: Article language: English refInfo: holdings: @attributes: islocal: N |
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