Distance remote Consenting for Children and Neonates in Research Studies V2
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Overview
This SOP describes the process for seeking informed consent for a neonate or child to potentially enter a clinical trial in circumstances where it is not possible for parents/legal guardians to come to the Norfolk and Norwich University Hospital to meet the clinical/research team in person and in time to allow the usual face-to-face consenting discussions
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ClinicalReference
Date Uploaded
27.12.2023Date Review
23.10.2026File Size
477KbClinical Guidelines
This guideline has been approved by the Trust's Clinical Guidelines Assessment Panel as an aid to the diagnosis and management of relevant patients and clinical circumstances. Not every patient or situation fits neatly into a standard guideline scenario and the guideline must be interpreted and applied in practice in the light of prevailing clinical circumstances, the diagnostic and treatment options available and the professional judgement, knowledge and expertise of relevant clinicians. It is advised that the rationale for any departure from relevant guidance should be documented in the patient's case notes.The Trust's guidelines are made publicly available as part of the collective endeavour to continuously improve the quality of healthcare through sharing medical experience and knowledge. The Trust accepts no responsibility for any misunderstanding or misapplication of this document.