Provision of information relating to cord blood distributed for transplant
22.—(1) This regulation applies to a licensee in relation to any unit of cord blood distributed by the licensee to an acute hospital service licensee for the purpose of transplant.
[S 389/2023 wef 26/06/2023]
(2) The licensee must, in relation to the unit of cord blood distributed, provide the results of the following to the acute hospital service licensee (including the transplanting clinician who transplants or intends to transplant the cord blood):
(a)
all screenings of the infant donor of the cord blood and the mother of that infant donor;
(b)
all tests conducted of the cord blood.
[S 389/2023 wef 26/06/2023]
(3) The licensee must, upon request by the acute hospital service licensee or the transplanting clinician, make available the following information to the acute hospital service licensee or transplanting clinician (as the case may be):
(a)
the medical history of the infant donor from whom the unit of cord blood was collected and the mother of that infant donor;
(b)
information relating to the licensee’s testing and processing of the unit of cord blood.
[S 389/2023 wef 26/06/2023]
(4) The licensee must obtain from the transplanting clinician, within such time as a Clinical Governance Officer considers appropriate after the transplant has taken place, the following information:
(a)
information concerning any adverse reaction arising from the transplant of the cord blood;
(b)
information about the recipient of the cord blood.
(5) This regulation is subject to any prohibition or restriction under any other written law or rule of law.