Victorian Consolidated Regulations
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Drugs, Poisons and Controlled Substances Regulations 2006 - SECT 41
Methods by which records are to be retained and retrieved
41. Methods by which records are to be retained and retrieved
(1) A person required to keep records under this Division must ensure that the
records of all transactions in Schedule 8 poisons or Schedule 9 poisons kept
by the person-
(a) are able to be readily sorted by poison or controlled substance; and
(b) show the true and accurate balance of each Schedule 8 poison and
Schedule 9 poison remaining in the person's possession after each
transaction; and
(c) show the name of the person carrying out the transaction.
Penalty: 50 penalty units.
(2) A person required to keep records under this Division must keep records
made by the person readily retrievable in English.
Penalty: 50 penalty units.
(3) A person required to keep records under this Division must retain a record
of each transaction in a Schedule 4 poison, Schedule 8 poison or Schedule 9
poison in a readily retrievable form for 3 years from the date of the
transaction.
Penalty: 50 penalty units.
(4) A person required to keep records under this Division must produce on
demand to an authorised officer all records required to be kept under this
Division.
Penalty: 50 penalty units.
(5) A person required to keep records under this Division must maintain the
records made by him or her of transactions in Schedule 8 poisons or Schedule 9
poisons in a manner that ensures that the records cannot be altered,
obliterated, deleted or removed without detection.
Penalty: 50 penalty units.
(6) An approved provider of an aged care service where there is a resident who
is receiving a high level of residential care who has been supplied, on
prescription, with a Schedule 4 poison, Schedule 8 poison or Schedule 9 poison
need not comply with subregulation (1) in relation to Schedule 8 poisons or
Schedule 9 poisons that are-
(a) supplied on prescription for a specific person; and
(b) supplied in tamper-evident compartments of dose administration
containers; and
(c) labelled by a registered medical practitioner, pharmacist, dentist or
nurse practitioner for administration at times specified on the label.
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