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The Therapeutic Goods Administration (TGA) has issued an infringement notice to a woman in Western Australia for alleged breaches of the Therapeutic Goods Act 1989 (the Act). The value of the infringement notice is $2,520.
The woman allegedly breached a condition of the Therapeutic Goods (Medical Devices—Accredited Pathology Laboratories) (COVID-19 Emergency) Exemption 2020 (the Exemption) by importing COVID-19 test kits that were not included in the Australian Register of Therapeutic Goods (ARTG) and were not being imported in relation to an authorised pathology laboratory as required by the Exemption. These products are classified as Class 3 in-vitro diagnostic (IVD) medical devices. COVID-19 test kits must not be imported into Australia, or manufactured or supplied in Australia, unless they are included in the ARTG or are subject to a relevant exemption, approval or authority.
Where medical devices are covered by the Exemption, the conditions of the Exemption must be complied with. A failure to do so is a criminal offence under section 41MNB of the Act and exposes the company or any relevant individual to a civil penalty under section 41MNC of the Act. For further information, see the TGA's advice on the legal supply of COVID-19 test kits.
The TGA takes action concerning unlawful activity
The TGA regulates all medicines, medical devices and biologicals under the Act. Considering the current COVID-19 pandemic, contraventions of the Act are a cause of serious concern for the TGA. Any alleged breaches relating to products supplied as part of Australia's response to the pandemic will be given the highest priority.
The regulatory scheme is important to the safety of Australians and the TGA investigates suspected illegal activity related to therapeutic goods. A range of compliance and enforcement actions detect, deter and address unlawful activity in relation to therapeutic goods. Where appropriate this can involve criminal or civil court proceedings, which may result in substantial penalties, fines or imprisonment.