Information sheets should be designed for each appropriate age range to reflect comprehension and development, for example: Assent requires a clear explanation (comprehensible rather than comprehensive) as consent will be sought from the parent. Where common law applies (all research not covered by the regulations), the law states that the age of majority is 18.īe clear in all documentation about whether you are seeking consent or assent (seeking the child’s agreement) and, if in doubt, contact the Research Governance, Ethics & Assurance Team.Ĭonsent requires a full explanation of the study. Where the Clinical Trial Regulations apply (ie for CTIMPs), a minor is defined as someone under the age of 16. consultee information sheet (for consultees of adults lacking capacity to consent).information sheet(s) for children/young people. ![]()
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