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SErIES IAEA HumAn HEAltH SErIES IAEA Hum

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Dosimetry for those subjected to radiation imaging as part of an imaging<br />

research protocol is an essential component of clinical radiological research<br />

activities.<br />

Dosimetry methods used to estimate foetal dose should be documented.<br />

5.1.5.3. Occupational dosimetry<br />

Although routine occupational monitoring is typically the responsibility of<br />

the RPO, certain situations may require additional personnel monitoring. This<br />

may be a specialized process under the supervision of the medical physicist. This<br />

includes additional personal monitoring for interventional fluoroscopy<br />

examinations, monitoring of pregnant staff, and monitoring incidents of<br />

accidental personnel exposures.<br />

5.1.6. Instrumentation and calibration<br />

The QA radiographer(s) and medical physicist should have access to<br />

appropriate calibrated instrumentation, phantoms and other test equipment to<br />

perform measurements and testing.<br />

In order to ensure the accuracy of dosimetry and QC measurements, the<br />

instruments used for testing must be calibrated at regular intervals against<br />

accepted standards. The use of an accepted field cross-checking methodology is<br />

encouraged as a cost effective way of maintaining acceptable dosimetry<br />

standards. The facility should have a calibration policy and a record of equipment<br />

calibration and equipment cross-checks.<br />

5.2. THE AUDIT PROGRAMME<br />

Annex III contains checklists for the following equipment-specific areas to<br />

assist the auditor in reviewing radiation protection, as well as the general safety<br />

and QC practices of the facility:<br />

—Plain radiography;<br />

—Fluoroscopy and image guided interventional procedures;<br />

—Mammography;<br />

—Computed tomography;<br />

—Dental radiography;<br />

—Ultrasonography;<br />

—Magnetic resonance imaging;<br />

—Screen–film systems and cassettes;<br />

53

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