Editing Informed consent (section)

===Medicine===
Informed consent is part of ethical [[clinical research]] as well, in which a human subject voluntarily confirms his or her willingness to participate in a particular [[clinical trial]], after having been informed of all aspects of the trial that are relevant to the subject's decision to participate. Informed consent is documented by means of a written, signed, and dated informed consent form.<ref>{{cite web|url=https://www.ich.org/fileadmin/Public_Web_Site/ICH_Products/Guidelines/Efficacy/E6/E6_R1_Guideline.pdf |title=Guideline For Good Clinical Practice |access-date=2018-09-24}}</ref>
In [[medical research]], the [[Nuremberg Code]] set a base international standard in 1947, in response to the ethical violation in the [[Holocaust]]. Standards continued to develop.  Nowadays, medical research is overseen by an [[ethics committee]] that also oversees the informed consent process.