For section 38 (4) (b) of the Act , all of the following information is prescribed—
(a) the name, gender and date of birth of the monitored person;
(b) the name and postal address of the licensee;
(c) the date the monitored person started to be monitored for any radiation doses received in relation to the carrying out of the radiation practice;
(d) if the monitored person stopped being monitored for any radiation doses received in relation to the carrying out of the radiation practice—the date the monitored person stopped being monitored;
(e) details of the basis for the monitored person being required to be provided with, or to wear, a personal monitoring device;
(f) the type of radiation to which the monitored person has been exposed in relation to the carrying out of the radiation practice;
(g) for each assessment of a personal monitoring device worn by the monitored person in relation to the carrying out of the radiation practice—(i) the period to which the assessment relates; and(ii) the estimated total effective dose, worked out under the assessment, for the monitored person for the period; and(iii) details of the methodology used in the assessment.