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Cancellation or suspensionRegulatory action due to The manufactured medicine is separate and distinct from the medicine included in the ARTG. As the presentation of the product was unacceptable, the certification made under s26A(2)(c) was incorrect. The goods also did not conform to a requirement relating to advertising applicable to the goods under Part 5-1 of the Act and did not conform to a standard applicable to the goods., effective 23/12/2013