Commonwealth Consolidated Regulations Commonwealth Consolidated Regulations(1) The committee's functions are, at the request of the Minister or Secretary, to provide advice and to make recommendations to the Minister or Secretary about one or more of the following matters:
(a) the safety, efficacy and manufacturing quality of a complementary medicine;
(b) the safety and quality of ingredients that are, or are proposed to be, included in a determination under subsection 26BB(1) of the Act for a listed complementary medicine;
(c) any requirements that are, or are proposed to be, included in a determination under subsection 26BB(1) of the Act in relation to ingredients for a listed complementary medicine;
(d) the registration or listing of a complementary medicine;
(e) the variation of an entry for a complementary medicine in the Register;
(f) the continued retention of a complementary medicine in, or the removal of a complementary medicine from, the Register;
(g) any other matter (whether or not related to a complementary medicine), including a matter related to standards.
(2) The Minister or Secretary may require the committee to give
its advice to other persons or bodies.