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Within this report, the term “equipment” has been interpreted to mean the main types of equipment used in diagnostic radiology, nuclear medicine and radiotherapy. This follows the precedent established in RP 91 (EC (1997b)). It is important to be aware that treatment of the whole installation is outside the scope of this report. Thus, the requirements for an acceptable physical building with shielding that will adequately protect staff, the public and patients, power supplies and ventilation have not been addressed. However, these are areas of growing concern in which the requirements have changed considerably as both equipment and. | EUROPEAN COMMISSION RADIATION PROTECTION N 162 Criteria for Acceptability of Medical Radiological Equipment used in Diagnostic Radiology Nuclear Medicine and Radiotherapy Directorate-General for Energy Directorate D Nuclear Safety Fuel Cycle Unit D4 Radiation Protection 2012 This report was prepared by Quality Assurance Reference Centre for the European Commission under contract N . ENER 10 NUCL SI2.581655 and represents those organisations views on the subject matter. The views and opinions expressed herein do not necessarily state or reflect those of the European Commission and should not be relied upon as a statement of the Commission s views. The European Commission does not guarantee the accuracy of the data included in this report nor does it accept responsibility for any use made thereof. Europe Direct is a service to help you find answers to your questions about the European Union Freephone number 00 800 6 7 8 9 10 11 Certain mobile telephone operators do not allow access to 00 800 numbers or these calls may be billed. More information on the European Union is available on the Internet http europa.eu . Luxembourg Publications Office of the European Union 2012 ISBN 978-92-79-27747-4 doi 10.2768 22561 European Union 2012 Reproduction is authorised provided the source is acknowledged. Printed in Luxembourg 2 FOREWORD Luxembourg October 2012 The work of the European Commission in the field of radiation protection is governed by the Euratom Treaty and the secondary legislation adopted under it. Council Directive 97 43 Euratom the Medical Exposure Directive MED is the legal act defining the Euratom requirements on radiation protection of patients and of other individuals submitted to medical exposure. The MED requires the adoption of criteria of acceptability for equipment in order to indicate when remedial action is necessary including if appropriate taking the equipment out of service . In 1997 the Commission issued publication Radiation Protection 91 RP91 .
