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Home » Australian Regulator Would Require Preapproval of Mainstream Device Ads
Australian Regulator Would Require Preapproval of Mainstream Device Ads
June 1, 2012
Medical devicemakers who advertise their products to consumers in Australia’s media would be required to get their advertisements preapproved, under a Therapeutic Goods Administration (TGA) proposal to extend a system currently limited to nonprescription drugs.