Identification and review of incidental or abnormal findings
37.—(1)  Subject to paragraph (2), a licensee must —
(a)ensure that the qualified person mentioned in regulation 35(1)(i) states in the clinical laboratory report or radiological report all incidental findings that are potentially clinically significant and abnormal findings; and
(b)bring the incidental or abnormal findings to the attention of the requestor.
[S 417/2023 wef 26/06/2023]
(2)  Paragraph (1) does not apply in relation to an incidental finding in any genetic test if the patient in respect of whom the clinical laboratory report is issued or the requestor informs the licensee that the patient does not wish to be informed of any incidental finding.
[S 417/2023 wef 26/06/2023]