Informed Consent FAQs - HHS.gov
网页Informed consent is legally effective if it is both obtained from the subject or the subject’s legally authorized representative and documented in a manner that is consistent with the HHS protection of human subjects regulations and with applicable laws of the jurisdiction in which the research is conducted.
How to obtain informed consent for research - PMC - National …
网页2018年3月22日 · In our modern ethical conception, all research conducted on humans must be pre-emptively accepted by the subjects themselves through the procedure known as informed consent, which is a process by which “a subject voluntarily confirms his or her willingness to participate in a particular trial, after having …
Obtaining and Documenting Informed Consent | Human …
网页2024年7月25日 · Obtaining consent involves explaining the research and assessing participant comprehension using a consent document, usually a written consent form or information sheet, as a guide for the verbal explanation of the study.
Informed Consent | New England Journal of Medicine
网页2017年3月2日 · Informed consent, which is ethically essential in most clinical research, respects persons’ rights to decide whether participation in the research is compatible with their interests,...
Consent - UW Research
网页QUICK GUIDE. While all stakeholders are encouraged to read and become familiar with this entire guidance, the following resources provide a summary of the most vital aspects of consent: Consent Overview [Five high-level consent considerations which must be a part of a meaningful informed consent process and form]
Informed Consent - StatPearls - NCBI Bookshelf
网页2023年6月5日 · Informed consent is the process in which a health care provider educates a patient about the risks, benefits, and alternatives of a given procedure or intervention. The patient must be competent to make a voluntary decision about whether to undergo the procedure or intervention.
Informed consent process: A step further towards making it …
网页Obtaining informed consent from patients participating in clinical research is an important legal and ethical imperative for clinical trial researchers. Although informed consent is an important process in clinical research, its effectiveness and validity are always a concern.
Informed Consent for Clinical Trials | FDA - U.S. Food and Drug ...
网页Learn what informed consent is and find out more information about patient rights when deciding to enroll in a clinical trials.
网页Obtaining genuine informed consent from research participants is best thought of as a process of sharing information and addressing questions and concerns, rather than simply obtaining a signature on a prescribed form.
Frequently Asked Questions About Electronic and Remote Consent
网页Remote consent (sometimes referred to as “teleconsent”) is a method of obtaining informed consent using a paper or electronic consent form where the study team and participant are not in the same physical location during the consent process.