ENER/D3/2021-253-2 SAMIRA Study on the Implementation of Council Directive 2013/59/Euratom Requirements for Medical Equipment with Respect to Monitoring and Control of Patient’s Radiation Exposures

Description

The specific objective of the study is to support Member States in the implementation of the Council Directive 2013/59/Euratom requirements for medical radiological equipment, with respect to controlling, recording and reporting of patients’ radiation exposures. Lot 1: The specific objective of the study is to support Member States in the implementation of the Council Directive 2013/59/Euratom requirements for medical radiological equipment, with respect to controlling, recording and reporting of patients’ radiation exposures. In order to achieve this objective, the study will: (a) collect and analyse up-to-date information on the implementation of the Council Directive 2013/59/Euratom requirements for medical radiological equipment, with respect to controlling, recording and reporting of patients’ radiation exposures; (b) develop best-practice guidance on the implementation of the above requirements; (c) discuss the results of the work with Member States, with the view of stimulating further national and EU-level efforts in this area. Please consult the procurement documents available at the address indicated in Section I.3). Lot 1: The specific objective of the study is to support Member States in the implementation of the Council Directive 2013/59/Euratom requirements for medical radiological equipment, with respect to controlling, recording and reporting of patients’ radiation exposures. In order to achieve this objective, the study will: (a) collect and analyse up-to-date information on the implementation of the Council Directive 2013/59/Euratom requirements for medical radiological equipment, with respect to controlling, recording and reporting of patients’ radiation exposures; (b) develop best-practice guidance on the implementation of the above requirements; (c) discuss the results of the work with Member States, with the view of stimulating further national and EU-level efforts in this area. Please consult the procurement documents available at the address indicated in Section I.3).