SOP 865 Study Specific Document Management

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Overview
The focus of this SOP will be on the management and control of study specific research documents produced mainly by the chief investigator and Sponsor including administrative clinical and data management documents which meet the criteria for essential documents as described in the ICH Guidelines for Good Clinical Practice
Categories
Clinical
Reference
Date Uploaded
17.12.2019
Date Review
09.12.2022
File Size
766Kb


Clinical 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.