Informed consent in clinical trials
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 participants’ understanding of IC conclude that recall and u...
| Main Authors: | , , |
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| Format: | Article |
| Language: | English |
| Published: |
South African Medical Association
2022-10-01
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| Series: | South African Journal of Bioethics and Law |
| Online Access: | https://samajournals.co.za/index.php/sajbl/article/view/301 |