SOP 310 – Development of PIS and ICF v3
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Overview
The purpose of this SOP is to outline the process for designing Participant Information Sheet PIS and Informed Consent Form ICF for a study. A PIS and ICF are essential to the process of obtaining informed consent from trial participants.
Categories
ClinicalReference
Date Uploaded
27.12.2023Date Review
03.10.2026File Size
577KbClinical 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.