Medicines, Poisons and Therapeutic Goods Act 2022
39Authorisation of clinical trials
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39 Authorisation of clinical trials
39 Authorisation of clinical trials
(1) The Health Secretary may authorise a person, or a class of persons, to carry out an activity involving a scheduled substance or other prescribed therapeutic goods for the purposes of a clinical trial.
(2) The carrying out of the activity is authorised if it is carried out in accordance with—
(a) conditions imposed by the Health Secretary, and
(b) the prescribed requirements.