HUMAN REPRODUCTIVE TECHNOLOGY ACT 1991 - SECT 21
HUMAN REPRODUCTIVE TECHNOLOGY ACT 1991 - SECT 21
21 . Code and directions, generally
Without limiting the
generality of section 14(1)(c), the Code, or directions, may make provision as
to —
(a) the
criteria by which the appropriateness of a proposed artificial fertilisation
procedure is to be assessed; and
(b) the
means of determining and evaluating the considerations which should or may be
taken into account before an artificial fertilisation procedure is commenced,
including the diagnostic procedures involved; and
(c) the
method by which, and the extent to which, donors or prospective donors of
human gametes, human eggs undergoing fertilisation or human embryos are to be
assessed or selected; and
(d) the
practice and procedures to be carried out in relation to the collection,
keeping, use and disposal of human gametes, human eggs undergoing
fertilisation or human embryos, or for securing that such eggs or embryos are
in a suitable condition for implantation; and
(e) the
responsibilities of persons carrying out any procedures to which this Act
applies; and
(f) the
establishment of a basis for determining questions as to the control of, and
the power to deal with or dispose of, human gametes, human eggs undergoing
fertilisation or human embryos; and
(g) the
means of disposal, or prohibitions or restrictions in respect of the disposal,
of human gametes, human eggs undergoing fertilisation or human embryos; and
(h)
limitations to be placed on the use of human gametes, human eggs undergoing
fertilisation or human embryos which may be donated by any one individual
donor; and
(i)
the means of identifying, for the purposes of sections 24
and 26, the person or persons on behalf of whom any human gametes, human eggs
undergoing fertilisation or human embryos are stored, kept for implantation or
developed which, in accordance with consents given, may be —
(i)
a woman or man; or
(ii)
a couple who are married, or in a de facto relationship
with each other whether they are different sexes or both female;
and
(j) the
circumstances in which any human egg undergoing fertilisation or human embryo
derived from the use of reproductive technology shall be allowed to succumb;
and
(k)
what, for the purposes of this Act, may constitute an authorised diagnostic
procedure in relation to any human egg undergoing fertilisation or human
embryo or an approved project of research, or may be carried out or performed
in any particular kind of research, and what shall not; and
(m) the
assessment of applications seeking approval to carry out any project of
research; and
(n) the
requirement that prior approval of an Institutional Ethics Committee specified
in, or ascertainable by reference to, those Rules, be a condition applicable
to any particular practice, kind of practice or procedure or kind of
procedure; and
(o) the
making, retention and confidentiality of records; and
(p) such
other matters relating to the practice of reproductive technology as may be
specified in, or are required by or to be carried out or determined in
accordance with, the regulations.
[Section 21 amended: No. 3 of 2002 s. 73; No. 17
of 2004 s. 15.]