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Medical devices reforms
Medical devices reforms
An Action Plan for Medical Devices
On 4 April 2019, the 'Action Plan for Medical Devices' was released.
Whilst the regulatory requirements in Australia are some of the most stringent in the world, more can be done to further strengthen the system, placing patient safety first.
The Action Plan is a three part strategy to:
- improve how new devices get on the market in Australia
- strengthen monitoring and follow up of devices already in use
- provide more information to patients about the devices they use
The Action Plan provides an overview of the current regulatory system, what actions are proposed and the timeframes for these.
It will fast track TGA's implementation of medical device reforms already underway and consult on new ways to improve transparency and increase public and health professional confidence in the regulatory system. Involving consumers in the process is critical, noting that decisions on new policies or changes to the Therapeutic Goods Act will be required from the Parliament prior to potential implementation.
The TGA has been tasked with providing more detail on how the actions outlined in the Plan could be implemented, engage and consult with consumers and other stakeholders so that they have input to implementation.
An emphasis of the Plan is to introduce more transparency by the TGA and that greater scrutiny occurs throughout the whole device lifecycle.
- Action Plan for Medical Devices
More detailed information on each of the strategies in the Plan and proposed consultations will be published in the near future
Reclassification of surgical mesh devices
- Reclassification of surgical mesh devices
From 1 December 2018, all new surgical mesh devices (including urogynaecological mesh devices) seeking approval from the TGA will need to meet the higher evidentiary requirements of a Class III medical device.
Patient implant cards and consumer device information leaflets
- Patient implant cards and consumer device information leaflets
From 1 December 2018, manufacturers of all new permanently implantable devices (other than those exempted) will need to provide patient implant cards and have a consumer device information leaflet, as part of new consumer information requirements.
Pre-market assessment of medical devices reforms
The TGA is implementing a series of medical device regulatory reforms increasing the rigour of pre-market assessment of higher risk medical devices, to assure the quality, safety and performance of these devices.
Further information on key reforms is available from:
- Reclassification of hip, knee and shoulder joint replacements
- Australian medical device manufacturers
- Increased scrutiny of medical devices
- Product names
- Regulation impact statement: Premarket assessment requirements for Australian manufactured medical devices
IVD medical devices reforms
Extension to the timeframe for the transition to the IVD regulatory framework
The current regulatory framework for in vitro diagnostic medical devices (IVDs) was introduced in 2010 via amendments to the Therapeutic Goods (Medical Devices) Regulations 2002 and the Therapeutic Goods Regulations 1990. The provisions included a 4-year transition period for IVDs supplied in Australia prior to 1 July 2010, with all such IVDs required to comply with the new requirements by 1 July 2014.
Due to difficulties encountered during the transition period, the TGA proposed an extension to the timeframe. An extension has now been made through amendments to those regulations. The new deadlines to demonstrate compliance with the IVD regulatory framework are summarised in the table below. They will come into effect immediately before 1 July 2014.
The new transitional provisions do not apply to any product that was supplied prior to 1 July 2010 and since this date, has been the subject of an application for inclusion in the Australian Register of Therapeutic Goods (ARTG) under Chapter 4 of the Therapeutic Goods Act 1989 that was rejected. These products cannot be legally supplied after 30 June 2014 unless they are included in the ARTG.
There is no annual charge for IVDs included in the ARTG under Chapter 4 of the Act for the 2013-2014 financial year. This exemption will continue to the end of the 2016-2017 financial year when the transition period ends.
|Deadline||Requirement for transitioning IVDs|
|31 August 2014||
Submission of an effective application1 for TGA conformity assessment certificates for:
For Class 4 IVDs an effective application needs to be made for a Quality Management System Certificate (either Full Quality Assurance Procedures or Production Quality Assurance Procedures) and a Design Examination or Type Examination Certificate for each individual Class 4 IVD.
|30 June 2015||
Submission of an effective application1 for inclusion in the ARTG for all commercial IVDs.
Provision has been made for supply of IVDs beyond 30 June 2015 if the TGA has not issued a conformity assessment certificate (in relation to an application received prior to 1 September 2014) by this date.
|30 June 2016||
Submission of an effective application1 for TGA conformity assessment certificates for laboratories that manufacturer Class 4 in-house IVDs.
For Class 4 in-house IVDs an effective application needs to be made for a Quality Management System Certificate (either Full Quality Assurance Procedures or Production Quality Assurance Procedures) and a Design Examination or Type Examination Certificate for each individual Class 4 in-house IVD.
|30 June 2017||
Submission of an effective application1 for inclusion in the ARTG for Class 4 in-house IVDs and notification of Class 1-3 in-house IVDs.
Provision has been made for supply of Class 4 in-house IVDs beyond 30 June 2017 if the TGA has not issued a conformity assessment certificate (in relation to an application received prior to 1 July 2016) by this date.
- An application is considered to be effective once the prescribed application fee has been paid.
If you require further information on the timeframe extension please email, firstname.lastname@example.org.