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Medicines and Poisons (Medicines) Regulation 2021
sec.110Contents of clinical protocol
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sec.110 Contents of clinical protocol
A prescriber must make a clinical protocol in writing and state the following information— the name of the prescriber; the place to which it relates; the class of persons who may administer a medicine under the protocol; the circumstances in which the protocol applies; 1 or more medicines to which the protocol applies; the way each medicine may be administered; the day, no later than 2 years after the protocol is made, by which the protocol must be reviewed.
- (a) the name of the prescriber;
- (b) the place to which it relates;
- (c) the class of persons who may administer a medicine under the protocol;
- (d) the circumstances in which the protocol applies;
- (e) 1 or more medicines to which the protocol applies;
- (f) the way each medicine may be administered;
- (g) the day, no later than 2 years after the protocol is made, by which the protocol must be reviewed.