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Voluntary informed consent and good clinical practice for clinical research in South Africa: Ethical and legal perspectives
Abstract
requirements for voluntary informed consent for clinical research participation in South Africa. International guidance documents reflect the minimum of the ethical requirements for the conduct of clinical research. Country-specific documents should be updated and aligned with relevant legislative and legal principles of that jurisdiction to ensure that research participants are adequately protected. The South African-specific guidance documents
therefore require revision to address these deficiencies.