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The Registration of Homoeopathic Veterinary Medicinal Products Regulations 1997

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Duties on qualified persons

26.—(1) A qualified person shall carry out the duties specified in Article 30 of Directive 81/851.

(2) Where the qualified person certifies a batch of a registered product in a register or equivalent document in accordance with Article 30.2 of Directive 81/851, he shall keep the register or equivalent document at the disposal of the relevant enforcement authority for a period of five years from and including the date on which the certification is made.

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