This consultation closed on 31 March 2019.
On this page: Invitation to comment | Consultation documents | Timetable | Submissions | Enquiries | What will happen | Privacy information
Invitation to comment
The Therapeutic Goods Administration (TGA) sought feedback on how personalised medical devices are regulated in Australia.
Over the past two decades, rapid advances in computing technology and materials science have driven exponential change in medical imaging technology, manufacturing technology, and (as a result) medical device technology. Advancing technology such as 3D printing is allowing more complex and, in some cases, higher risk medical devices to be manufactured for an individual patient, and is also allowing point of care manufacture of these personalised medical devices.
The proposed changes set out in this consultation seek to better regulate personalised medical devices, including the introduction of new definitions. The purpose of this consultation, which follows on from an earlier public consultation and public forums in 2017 and 2018, is to understand the impact that the proposed changes will have on the medical devices industry, health care professionals, and patients.
Consultation documents
How to access a pdf or Word document
- Consultation: Proposed regulatory scheme for personalised medical devices, including 3D-printed devices (pdf,298kb)
- Consultation: Proposed regulatory scheme for personalised medical devices, including 3D-printed devices (docx,121kb)
Timetable
Document released for consultation on Wednesday, 13 February 2019.
Interested parties should respond by close of business Sunday, 31 March 2019.
Feedback will be released following consideration of submissions. (See 'What will happen').
Submissions
Submissions must be relevant to the proposed amendments and questions detailed within the consultation paper.
In addition, submissions may include information on:
- Suggested improvements.
- Whether or not you support the proposals, including suggestions for alternatives.
- An assessment of how the proposal will impact on you.
Enquiries
Any questions relating to submissions should be emailed to devicereforms@tga.gov.au
What will happen
All submissions will be placed on this website unless marked confidential or indicated otherwise in the submission form (see Privacy information).
Submissions will be reviewed by the TGA and feedback on submissions will be provided through this website.
Recommendations made by the TGA following consideration of submissions from interested parties will be published on the TGA website as outcomes.
Privacy information
- The TGA collects your personal information in this submission in order to:
- contact you if the TGA wants to seek clarification of issues raised in your submission or to check whether you consent to certain information that you have provided being made publicly available.
- help provide context about your submission (e.g. to determine whether you are an individual or a director of a company or representing an interest group).
- seek feedback about how the consultation was undertaken.
- Please do not include personal information about other individuals in the body of your submission. Personal information in this context means information or an opinion about an individual whose identity is apparent, or can reasonably be ascertained, from the information or opinion.
- More information on consultations and privacy is included in the submission form and on our website.