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 ...

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, ...

Obtaining informed consent is most often accomplished through an informed consent form, which documents the information regarding the research the subject is being given to help him/her make the ...

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 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, ...