(1) The director-general must keep a register about the supply and disposal of approved substances for the purpose of contacting any person the director-general considers appropriate in relation to an approved substance that has been supplied under this Act.
(2) The register—
(a) must include any information prescribed by regulation; and
(b) may include any other information the director-general considers appropriate.
(3) The director-general may correct any mistake, error or omission in the register.
(4) The director-general may give information in the register to a relevant entity if—
(a) the relevant entity requests the information; and
(b) the director-general is satisfied that the information is relevant to the exercise of the relevant entity's functions.
(5) In this section:
"medicines and poisons inspector"—see the Medicines, Poisons and Therapeutic Goods Act 2008
"relevant entity" means—
(a) the board; or
(b) a
medicines and poisons inspector.