{"id":4406,"date":"2024-01-08T13:58:14","date_gmt":"2024-01-08T18:58:14","guid":{"rendered":"https:\/\/www.rochester.edu\/ohsp\/?page_id=4406"},"modified":"2024-02-07T14:59:32","modified_gmt":"2024-02-07T19:59:32","slug":"documentation","status":"publish","type":"page","link":"https:\/\/www.rochester.edu\/ohsp\/resources\/consent\/documentation\/","title":{"rendered":"Documentation"},"content":{"rendered":"<p>It\u2019s important to ensure you document informed consent in a manner that is legal and valid. To meet that aim, study teams often assume that documenting consent is as simple as obtaining a subject\u2019s signature on the form. Although a subject\u2019s signature is a vital component in the documentation the process, considering consent documentation more broadly, as a process, as you would any other essential or required study documentation will help ensure success.<\/p>\n","protected":false},"excerpt":{"rendered":"<p>It\u2019s important to ensure you document informed consent in a manner that is legal and valid. To meet that aim, study teams often assume that documenting consent is as simple&hellip;<\/p>\n","protected":false},"author":36,"featured_media":0,"parent":4386,"menu_order":0,"comment_status":"closed","ping_status":"closed","template":"","meta":{"footnotes":""},"class_list":["post-4406","page","type-page","status-publish","hentry"],"acf":[],"yoast_head":"<!-- This site is optimized with the Yoast SEO plugin v27.3 - https:\/\/yoast.com\/product\/yoast-seo-wordpress\/ -->\n<title>Documentation of Informed Consent - Office for Human Subject Protection - University of Rochester<\/title>\n<meta name=\"description\" content=\"Guidance to ensure that human subject researchers document informed consent in a manner that is legal and valid. 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