Assisted Reproductive Treatment Regulations 2019
Sch 4Information to be recorded in Register of pre‑1988 donor treatment procedures kept by registered ART provider
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Schedule 4—Information to be recorded in Register of pre‑1988 donor treatment procedures kept by registered ART provider
Regulation 15
1 Information relating to donors of gametes used in pre-1988 donor treatment procedures
The following information is prescribed in relation to each pre-1988 donor of gametes—
(c) the date of birth of the donor;
(d) the donor's place of birth (suburb or town and country);
(e) the sex of the donor;
(f) any other name by which the donor is or has been known;
(g) the donor's residential address and contact telephone number;
(h) the date on which the donor produced the gametes;
(i) the place at which the donor produced the gametes;
(j) if the gametes were not produced at the premises of the registered ART provider, the date on which the gametes were received by the registered ART provider;
(o) any known genetic abnormality of the donor and, if available, any results of tests undertaken in relation to that abnormality;
(p) the donor's hair colour;
(q) the donor's eye colour;
(r) the donor's marital status;
(s) the donor's occupation;
(t) the donor's education;
(u) the donor's interests;
(v) the number of women who have given birth to children conceived using the donor's gametes, including the donor and any current or former partner of the donor;
(w) the total number of children born as a result of treatment procedures carried out by the registered ART provider using the donor's gametes;
(x) whether the donor has donated gametes to any other registered ART provider or to a doctor.
2 Information relating to each woman on whom a pre‑1988 donor treatment procedure was carried out by a registered ART provider and the partner, if any, of each woman
(1) The following information is prescribed in relation to each woman on whom a pre-1988 donor treatment procedure was carried out by a registered ART provider—
(a) the full name of the doctor who performed the procedure;
(b) the full name of the woman;
(c) the date of birth of the woman;
(d) the place of birth of the woman (suburb or town and country);
(e) any known genetic abnormality of the woman and, if available, any results of tests undertaken in relation to that abnormality;
(f) if the woman gave birth to a child as a result of a previous treatment procedure—
(i) the name of the registered ART provider or doctor who carried out the treatment procedure; and