Impact of amendments to the application process for inclusion of Class I medical devices in the Australian Register of Therapeutic Goods (ARTG)

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Closes 1 Oct 2021

Survey Contents

You may answer all or selective questions. Only the ‘Publishing Your Response’ section is mandatory - this must be completed in order to submit a response (HINT: it is the only section with a 'Finish' button at the end).

You will find a list of questions about yourself under the section titled 'Respondent Information'. The questions in this section are not mandatory and can be skipped. Telling us more about you and your interest in this subject, allows us to better understand your unique needs and perspective.

Thank you very much for your feedback - we look forward to learning more about your issues and ideas about the changes made to the process for including Class I non-sterile, non-measuring devices, and Class 1 in vitro diagnostic (IVD) devices in the ARTG.