Reporting Ad-hoc demand work to Clinical Engineering V1.2
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Overview
The policy has been written to ensure that trust clinical staff understand the process of reporting any issues with Medical Devices to Clinical Engineering in order to receive technical support to enable a satisfactory rectification of any medical equipment issues.
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ClinicalReference
Date Uploaded
13.12.2023Date Review
22.11.2025File Size
400KbClinical 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.