SOP 315 – Obtaining written Informed Consent from Competent Adults in Clinical Trials V2
Preview
Overview
The purpose of this SOP is to describe the process for obtaining written Informed Consent for healthcare research sponsored by the NNUH and UEA that is conducted under the Research Governance Framework 2nd edition 2005 or its successor.
Categories
ClinicalReference
Date Uploaded
21.02.2023Date Review
02.02.2026File Size
358KbClinical 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.