S.L. 585.1 Art. 66Optimisation.

(1) All doses due to medical exposure for radiodiagnostic, interventional radiology, planning, guiding and verification purposes are to be kept as low as reasonably achievable consistent with obtaining the required medical information, taking into account economic and societal factors.

(2) For all medical exposure of patients for radiotherapeutic purposes, exposures of target volumes shall be individually planned and their delivery appropriately verified taking into account that doses to non-target volumes and tissues shall be as low as reasonably achievable and consistent with the intended radiotherapeutic purpose of the exposure.

(3) (a) The Commission shall establish and regularly review national diagnostic reference levels for radio-diagnostic examinations, having regard to the current European diagnostic reference levels where available, and where appropriate, for interventional radiology procedures, and the availability of guidance for this purpose.

(b) An undertaking shall ensure that diagnostic reference levels for their radio-diagnostic examinations, and where appropriate for interventional radiology procedures, are established, regularly reviewed and used, having regard to the national diagnostic reference levels where available..

(4) For each medical or biomedical research project involving medical exposure:

(a) the individuals concerned participate voluntarily;

(b) these individuals are informed about the risks of exposure;

(c) a dose constraint is established for individuals for whom no direct medical benefit is expected from exposure;

(d) in the case of patients who voluntarily accept to undergo an experimental medical practice and who are expected to receive a diagnostic or therapeutic benefit from an individual basis by the practitioner and/or referrer prior to the exposure taking place.

(5) Undertakings shall ensure that the optimisation includes the selection of equipment, the consistent production of adequate diagnostic information or therapeutic outcomes, the practical aspects of medical radiological procedures, quality assurance, and the assessment and evaluation of patient doses or the verification of administered activities, taking into account economic and societal factors.

(6) Undertakings shall ensure that:

(a) a dose constraints of not more than 1.5mSv per five years is applied exposure of carers and comforters, where appropriate;

(b) appropriate guidance is established for the exposure of carers and comforters.

(7) In the case of a patient undergoing treatment or diagnosis with radionuclides, the undertaking, shall ensure that the patient or their representative is provided with information on the risks of ionising radiation and appropriate instructions with a view to restricting doses to persons in contact with the patient as far as reasonably achievable. For therapeutic procedures these shall be written instructions.

These instructions shall be handed out before leaving the hospital or clinic.