(1) An authorised psychedelic psychiatrist must not authorise the administration of Schedule 8 MDMA or Schedule 8 psilocybine unless—
(a) the administration is for the medical treatment of a person other than the psychiatrist; and
(b) that person is under the psychiatrist's care; and
(c) the psychiatrist has taken all reasonable steps to ensure a therapeutic need exists for that poison; and
(d) the administration is authorised not merely for the purpose of supporting the drug dependence of a person; and
(e) the psychiatrist has taken all reasonable steps to ascertain the identity of the person to whom the poison is to be administered; and
(f) the psychiatrist has complied with regulation 17A.
Penalty: 100 penalty units.
(2) A registered medical practitioner must not authorise the administration of Schedule 8 MDMA or Schedule 8 psilocybine to a participant in a clinical trial that is approved by or notified to the Commonwealth Secretary under the Therapeutic Goods Act 1989 of the Commonwealth and approved by a human research ethics committee unless—
(a) the medical practitioner is not the participant in the clinical trial; and
(b) the administration is for the purpose of the clinical trial; and
(c) the participant is under the medical practitioner's care; and
(d) the administration is authorised not merely for the purpose of supporting the drug dependence of the participant; and
(e) the medical practitioner has taken all reasonable steps to ascertain the identity of the participant to whom the poison is to be administered; and
(f) the medical practitioner has complied with regulation 17A.
Penalty: 100 penalty units.