Poisons and Therapeutic Goods Regulation 2008
94AAAuthority required for supply for clinical trials
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94AA Authority required for supply for clinical trials
94AA Authority required for supply for clinical trials
A medical practitioner must not supply a type C unregistered drug of addiction unless—
(aa) the prescription is for the purposes of a clinical trial, and
(a) the medical practitioner holds an authority under Division 4 of Part 8 of this Regulation that authorises the practitioner to supply that type C unregistered drug of addiction for the purposes of a clinical trial, and
(b) the supply of the unregistered drug is in accordance with the authority.
Maximum penalty—20 penalty units
cl 94AA: Ins 2019 (477), Sch 1 [3]. Am 2020 (111), Sch 1[4].