Informed consent in clinical trials

Autor: Kovane, G P, Nikodem, V C, Khondowe, O

Publikováno v: South African Journal of Bioethics and Law; Vol. 15 No. 2 (2022); 48-53
South African Journal of Bioethics and Law, Volume: 15, Issue: 2, Pages: 48-53, Published: OCT 2022

Background. Informed consent (IC) is not only a regulatory but also an ethical requirement to participate in any clinical trial. It is essential to determine that research participants understand what they consent to. Studies that evaluate participan

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::23c1918bbb0c1bf20394d6234187b9c0
https://www.ajol.info/index.php/sajbl/article/view/235219

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