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reg 431

Authorisation conditions for non-controlled medicines research and education—Act, s 44 (1) (b) and (2) (b)

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Chapter 9Other medicines authorisations
Part 9.3Medicines authorisations for corrections functions

431 Authorisation conditions for non-controlled medicines research and education—Act, s 44 (1) (b) and (2) (b)

A scientifically qualified person’s authorisation under section 430 is subject to the following conditions:

(a)

the person has written approval for the conduct of the authorised activity from the person in charge of—

(i)

the recognised research institution; or

(ii)

a faculty or division of the institution;

(b)

if the recognised research institution employing the person is a hospital operated by the Territory—

(i)

a requisition for the relevant medicine issued by the person complies with section 55 (General requirements for written requisitions) and section 56 (Particulars for requisitions); and

(ii)

the requisition is for an amount of the medicine approved in writing by the person in charge; and

(iii)

the requisition is for an amount of the medicine used solely for the purpose approved in writing by the person in charge;

(c)

if the person is employed at a recognised research institution other than a hospital operated by the Territory—

(i)

a purchase order for the relevant medicine complies with section 62; and

(ii)

the purchase order is for an amount of the medicine approved in writing by the person in charge;

(d)

the medicine is obtained from someone who is authorised to supply the medicine to the person.

Part 9.5 Authorisations under medicines licences

Division 9.5.1 Controlled medicines research and education program licence authorisations

Note 1 For authorisation for research and education for other medicines, see pt 9.4.

Note 2 For other provisions about controlled medicines research and education program licences, see pt 14.2.

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Section 431 — Authorisation conditions for non-controlled medicines research and education—Act, s 44 (1) (b) and (2) (b) — Medicines, Poisons and Therapeutic Goods Regulation 2008 (Australian Capital Territory) — Barrister AI