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Although exempt research is exempt from some of the federal regulations, in most cases of interaction with participants, a consent process is indicated. It’s important to understand that even though ...
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Electronic consent demonstrates potential to overcome 'key barrier' in stroke trial recruitment - MSNOutlining the results of their research, the team states that eConsent was utilized for 173 (93 in person, 80 remote) of a total of 514 participants (33.7%), while the remaining 341 (337 in person ...
Print form — Media Consent Form 2014 (PDF) Sign form — Before your media can be made public (uploaded to YouTube and/or posted on the Bates website), individuals featured within that media must first ...
Obtaining informed consent is more than getting a signature on a form. Informed consent is one of the primary ethical considerations underlying research with human subjects. ALL human subject research ...
The Revised Common Rule requires all clinical trials to post an unsigned consent form on a publicly available website. The Revised Common Rule is in effect for studies approved on or after January 21, ...
326. Short Form Written Consent Documentation | Research Integrity & Security | University of Nevada, Reno ...
Office of Research and Innovation Western Michigan University Kalamazoo MI 49008-5456 USA (269) 387-8298. ... Note: There can be no exculpatory language anywhere in the form. Administering the consent ...
The principle of respect for persons demands that participants enter the research voluntarily and with adequate information. When deceptive methodologies are used, participants are given incomplete or ...
The plan for obtaining consent must be included in the Human Subjects Protocol. Investigators may request a waiver or alteration of the informed consent process or waiver of consent documentation, ...
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