After section 50 insert:
50A—Limited and controlled release applications
(1) This section
applies to an application for a licence if the Regulator is satisfied
that—
(a) the
principal purpose of the application is to enable the licence holder, and
persons covered by the licence, to conduct experiments; and
(b) the
application proposes, in relation to any GMO in respect of which dealings are
proposed to be authorised—
(i)
controls to restrict the dissemination or persistence of
the GMO and its genetic material in the environment; and
(ii)
limits on the proposed release of the GMO; and
(c) the
Regulator is satisfied that the controls and limits are of such a kind that it
is appropriate for the Regulator not to seek the advice referred to in
section 50(3).
(2) For the purposes
of subsection (1)—
"controls", in relation to restricting the dissemination or persistence of a
GMO and its genetic material in the environment, include the following:
(a)
specified methods for disposal of the GMO or its genetic material;
(b) data
collection requirements, including studies to be conducted about the GMO or
its genetic material;
(c) a
restricted geographic area in which the proposed dealings with the GMO or its
genetic material may occur;
(d)
compliance, in relation to dealings with the GMO or its genetic material,
with—
(i)
a code of practice issued under section 24; or
(ii)
a technical or procedural guideline issued under section
27.
(3) For the purposes
of subsection (1)—
"limits", in relation to the release of a GMO that is proposed to be
authorised by a licence, includes limits on any of the following:
(a) the
scope of the dealings with the GMO;
(b) the
scale of the dealings with the GMO;
(c) the
locations of the dealings with the GMO;
(d) the
duration of the dealings with the GMO;
(e) the
persons who are to be permitted to conduct the dealings with the GMO.
(4) In deciding
whether the principal purpose of an application is to enable the licence
holder, and persons covered by the licence, to conduct experiments, the
Regulator—
(a) must
have regard to whether the applicant proposes that any or all of the following
be authorised by, and done under, the licence:
(i)
testing hypotheses;
(ii)
gaining scientific or technical knowledge;
(iii)
gaining data for regulatory purposes, or for product
development or marketing; and
(b) may
have regard to any other matter that the Regulator considers to be relevant.
Note—
This section differs from section 50A of the Commonwealth Act.