Commonwealth Consolidated Regulations(1) For paragraph 99ADC (1) (c) of the Act, the information mentioned in regulation 37H must be provided within 6 weeks after the end of each reporting period for the brand of the pharmaceutical item.
(2) Subject to subregulations (3) to (6) and regulation 37JA, a reporting period for a brand of a pharmaceutical item is:
(a) the period of 6 months ending at the end of 31 March of each year and 30 September of each year; and
(b) each successive period of 6 months in which the brand is subject to the price disclosure requirements.
(3) However, the first reporting period for a relevant brand to which regulation 37ED applies:
(a) begins on the relevant day mentioned in regulation 37ED for the relevant brand; and
(b) ends at the end of the first of the following dates to happen after the relevant day:
(i) 31 March;
(ii) 30 September.
(4) Also, the first reporting period for a relevant brand in the relevant disclosure cycle mentioned in regulation 37F to which that regulation applies:
(a) begins on the relevant day mentioned in regulation 37F; and
(b) ends at the end of:
(i) if the other brand mentioned in regulation 37F is in the interim supplementary disclosure cycle or a supplementary disclosure cycle A or supplementary disclosure cycle B -- the reporting period for the other brand; or
(ii) in any other case -- the first of the following dates to happen after the relevant day:
(A) 31 March;
(B) 30 September.
(5) Also, the first reporting period in the data collection period in the first main disclosure cycle for a brand of a pharmaceutical item to which regulation 37EG applies:
(a) begins on 1 February in the year the brand moves to the main disclosure cycle; and
(b) ends at the end of 31 March in the year.
(6) Also, the first reporting period in the data collection period in the first main disclosure cycle for a brand of a pharmaceutical item to which regulation 37EH applies:
(a) begins on 1 June in the year the brand moves to the main disclosure cycle; and
(b) ends at the end of 30 September in the year.
Note For transitional arrangements, see Part 2 of the National Health (Pharmaceutical Benefits) Amendment Regulations 2010 (No. 5).
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