(1) The Director-General may register a trade name product in accordance with section 21, subject to all or any of the following conditions:
(a) A condition on the use of the trade name product:
(b) A condition requiring the trade name product to originate from specified sources:
(c) A condition restricting the importation to certain classes of persons:
(d) A condition specifying the labelling, advertising, or other information requirements for the trade name product:
(e) A condition specifying standards of competence for manufacturers, sellers, purchasers, or users of the trade name product:
(f) a condition requiring an operating plan approved by the Director-General under section 28 to be followed when importing, manufacturing, selling, distributing, storing, transporting, or using the trade name product:
(g) A condition on the packaging or storage of the trade name product:
(h) A condition specifying standards of quality, purity, and potency for the trade name product:
(i) A condition specifying procedures for testing the trade name product for quality, purity, or potency:
(j) A condition requiring systems to be approved to ensure that the trade name product meets specified standards of quality, purity, and potency, and procedures for auditing those systems:
(ja) a condition requiring that persons who import, manufacture, sell, or use a trade name product must do so under the authority of, and in compliance with any requirements of, a recognised person or any class or description of recognised persons:
(jb) a condition requiring that persons who authorise the use of a trade name product must do so in compliance with any requirements specified by the Director-General:
(k) A condition requiring information and records to be kept and to be reported, or made available on request, to the Director-General, or an ACVM officer:
(l) A condition requiring samples of the trade name product to be taken and tested and the test results to be made available on request to the Director-General, or an ACVM officer:
(m) Such other conditions as the Director-General considers necessary to achieve the purposes of this Act.
(2) A condition imposed in accordance with this section may apply to any specified class of person or to every person who imports, manufactures, sells, or uses a trade name product; and every person to whom a condition applies must comply with that condition.
(3) The Director-General must, when imposing conditions in accordance with this section, take into account conditions imposed in any prescribed countries on the trade name product.
(4) The Director-General must not impose conditions under this section if he or she is satisfied that the relevant risks that the conditions would address are already adequately managed by conditions or controls imposed by or under any other Act.
(5) The specificity of the conditions listed in paragraphs (a) to (l) of subsection (1) does not limit the conditions that may be imposed under paragraph (m) of that subsection.
Section 23(1)(f): substituted, on 18 October 2007, by section 16(1) of the Agricultural Compounds and Veterinary Medicines Amendment Act 2007 (2007 No 93).
Section 23(1)(ja): inserted, on 18 October 2007, by section 16(2) of the Agricultural Compounds and Veterinary Medicines Amendment Act 2007 (2007 No 93).
Section 23(1)(jb): inserted, on 18 October 2007, by section 16(2) of the Agricultural Compounds and Veterinary Medicines Amendment Act 2007 (2007 No 93).
Section 23(1)(k): amended, on 18 October 2007, by section 16(3) of the Agricultural Compounds and Veterinary Medicines Amendment Act 2007 (2007 No 93).
Section 23(1)(l): amended, on 18 October 2007, by section 16(3) of the Agricultural Compounds and Veterinary Medicines Amendment Act 2007 (2007 No 93).
Section 23(4): added, on 18 October 2007, by section 16(4) of the Agricultural Compounds and Veterinary Medicines Amendment Act 2007 (2007 No 93).
Section 23(5): added, on 18 October 2007, by section 16(4) of the Agricultural Compounds and Veterinary Medicines Amendment Act 2007 (2007 No 93).