35.—(1) A clinical laboratory report or radiological report mentioned in regulation 34(1) or (2), other than a clinical laboratory report mentioned in paragraph (2), must contain all of the following information:
(a)
the following information about the licensee issuing the report:
(i)
the licensee’s name and the business name (if different from the licensee’s name) by which the licensee provides the applicable service;
(ii)
the licensee’s address;
[S 417/2023 wef 26/06/2023]
(b)
all of the following identifying information:
(i)
the patient’s name;
(ii)
the patient’s identification number or passport number;
(iii)
where the information in sub‑paragraphs (i) and (ii) is not known to the licensee — other information identifying the patient;
(c)
subject to paragraph (1A), the address of the premises at which or the vehicle number of the approved conveyance in which the test or radiological examination is conducted;
[S 417/2023 wef 26/06/2023]
(d)
the date the test or radiological examination is conducted;
(e)
the name of the requestor;
(f)
the description and findings of the test or radiological examination;
(g)
for a clinical laboratory report —
(i)
where the information is known to the clinical laboratory service licensee — the date and time the specimen was derived from the patient;
(ii)
[Deleted by S 417/2023 wef 26/06/2023]
(iii)
for a tissue specimen — the anatomical site of the specimen; and
(iv)
any other necessary information for the interpretation of results, including the established norms and ranges applicable to the test results;
(h)
the date the report is issued;
[S 417/2023 wef 26/06/2023]
(i)
the name and signature (including an electronic signature) of the qualified person certifying the test results or interpreting and reporting the findings of the radiological examination.
(1A) Where the premises at which the test or radiological examination is conducted are temporary premises that are residential premises, the licensee issuing the report may, instead of stating the address of those premises in the clinical laboratory report or radiological report (as the case may be), indicate that the test or radiological examination was conducted at residential premises.
[S 417/2023 wef 26/06/2023]
(2) A clinical laboratory report mentioned in regulation 34(1) issued for any test in relation to COVID‑19 must contain the information set out in paragraph (1)(b), (d), (f) and (h).
(3) Where a licensee appoints or engages another person (A) to conduct a test or radiological examination on the licensee’s behalf under regulation 41, the clinical laboratory report or radiological report (as the case may be) must also include the following:
(a)
A’s name;
(b)
the address of the premises in which the test or radiological examination (as the case may be) was performed;
(c)
the original clinical laboratory report or radiological report (as the case may be) issued by A, if any.