Failing the vulnerable: Three new consent norms that will undermine health research with children

Southern African Journal of HIV Medicine

Field Value
Title Failing the vulnerable: Three new consent norms that will undermine health research with children
Creator Strode, Ann Richter, Marlise Wallace, Melissa Toohey, Jacintha Technau, Karl
Subject Health Research; Law; Ethics Legal; Social Sciences HIV AIDS; Children; Law; Consent; legislation; proxy; parental consent
Description The South African National Health Act (No. 61 of 2003) provides a legal framework for the regulation of the health system across the country. Within the Act, section 71 introduces a number of legal norms relating to research or experimentation with human subjects, including research on HIV prevention and treatment. These norms have been criticised for the negative impact they will have on research involving children. This article describes three of the new consent requirements in section 71 of the Act. It shows, using a range of case studies, how important HIV-related research will be halted or undermined if the current provisions are implemented. The article argues that the new consent requirements are out of step with other statutory provisions and ethical guidelines, and as a result they will exclude a large population group – children in diverse settings – from much-needed evidence-based healthcare interventions. The article concludes with a clarion call for support of advocacy on this issue with the Minister of Health and the Health Portfolio Committee.
Publisher AOSIS
Date 2014-05-23
Type info:eu-repo/semantics/article info:eu-repo/semantics/publishedVersion —
Format application/pdf
Identifier 10.4102/sajhivmed.v15i2.18
Source Southern African Journal of HIV Medicine; Vol 15, No 2 (2014); 46-49 2078-6751 1608-9693
Language eng
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Rights Copyright (c) 2014 Ann Strode, Marlise Richter, Melissa Wallace, Jacintha Toohey, Karl Technau