Medicines, Poisons and Therapeutic Goods Regulation 2008
666Labelling of supplied manufacturer’s packs of low and
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666 Labelling of supplied manufacturer’s packs of low and moderate harm poisons—Act, s 60 (1) (c) (i) and (2) (c) (i) A manufacturer’s pack of a supplied low harm poison or moderate harm poison must be labelled in accordance with— (b) a relevant law. Note A manufacturer’s pack of a low or moderate harm poison supplied may also be labelled in accordance with an approval under the Act, s 193 (Approval of non-standard packaging and labelling) (see Act, s 60 (1) (c) (ii) and (2) (c) (ii)).
Part 17.1 Overview of dangerous poisons authorisations Chapter 17 Dangerous poisons Part 17.1 Overview of dangerous poisons 670 General overview of authorisations for dangerous (1) The Act requires that a person must not deal with a dangerous poison in a particular way unless the person is authorised to deal with the poison. the Act, s 35 about obtaining certain substances (which include dangerous poisons) Note The Act, s 19 sets out when a person deals with a dangerous poison. (2) The Act, section 20 sets out when a person is authorised to deal with a dangerous poison. (3) This regulation authorises certain dealings with dangerous poisons. Note An authorisation is not required to deal with the following: • a substance excluded from the medicines and poisons standard by the standard; • a substance mentioned in the medicines and poisons standard, sch 7 if the schedule does not apply to the substance because of an exception in the standard. (4) An authorisation under this regulation may be subject to limitations. a purchase order issued by a person mentioned in sch 4, col 2 must comply with s 721 (see s 690 (2) (c)) Note For the power to impose other restrictions, see the Act, ch 8.
Overview of dangerous poisons authorisations Part 17.1