Medicines, Poisons and Therapeutic Goods Act 2008
88Form of licences
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88 Form of licences (1) A licence must be in writing and include the following information: (a) what licence it is or the dealings with regulated substances or regulated therapeutic goods authorised by the licence; (b) the regulated substances or regulated therapeutic goods to which the licence relates; (c) the full name of the licence-holder; (d) the licence-holder’s ABN (if any); (e) if the licence-holder is a corporation—the corporation’s ACN; (f) if applicable, the location of the premises where the licence-holder is authorised to deal with a regulated substance or regulated therapeutic good under the licence; (g) if applicable, the name of each individual who is to supervise the dealings authorised under the licence; (h) any conditions included in the licence by the chief health officer; Note See s 90 to s 92 for conditions included in a licence by the chief health officer.
(i) a unique identifying number; (j) when the term of the licence ends; (k) any other information prescribed by regulation. (2) For this Act, the conditions mentioned in subsection (1) (h) may be included in a separate document and, if they are, the separate document forms part of the licence.