AUDITRAD is an expanded version of Esperanto – ESR’s Guide to Clinical Audit. With 33 brand new audit templates, 55 templates from previous editions revised and updated, and refreshed guideline expanded on important and current topics like usage of AI tools, AUDITRAD is a comprehensive and up-to-date tool, ready to use by radiology departments across Europe. With a blank template, all users of AUDITRAD are invited to take the booklet to the next level and create their own audit templates according to their own needs. AUDITRAD is a joint effort of the CLAUD-IT EU4Health project consortium, ESR members, and other leading experts in respective fields.
This updated Guide to Clinical Audit presents a comprehensive approach to clinical audit. It contains variety of tools and support material to implement clinical audit in radiology especially in light of the EU requirements such as the Basic Safety Standards Directive (Council Directive 2013/59/Euratom), and the Commission Recommendation (EU) 2024/1112.
*The AUDITRAD guide is currently under review by the European Commission.
NuCline is a comprehensive guide to clinical audits in nuclear medicine designed to support best practices, regulatory compliance and quality improvement by aligning with European guidelines such as Commission Recommendation (EU) 2024/1112. The European legal framework for clinical audits in nuclear medicine is governed by the BSSD, ensuring high standards of radiation protection and patient safety, with the EANM playing a key role in promoting audits as a tool for continuous quality improvement and regulatory compliance across Europe.
NuCline outlines the EANM’s approach and ongoing efforts to support clinical audits in nuclear medicine, emphasizing their importance for quality and compliance. It also serves as a guideline to conducting clinical audits, featuring multiple audit templates developed by experts from the CLAUD-IT consortium that address key topics such as clinical practices, quality control of nuclear medicine equipment, radiopharmacy and regulatory audits.