Reviewing Conformity Assessment procedures

Project overview

We have been systematically reviewing the way medical devices are regulated. 

This has been guided by An Action Plan for Medical Devices. The Action Plan is a three-part strategy to strengthen Australia’s regulatory system while continuing to be patient focused and have greater transparency. 

The Australian Government is committed to improve how medical devices are regulated by internationally aligning our regulatory framework, wherever possible, and by participating in the Medical Devices Single Audit Program (MDSAP). 

We have been reviewing where alignment should occur with the conformity assessment procedures of the European Regulation 2017/745 on medical devices (MDR) and the European Regulation 2017/746 for in vitro diagnostic medical devices (IVDR).

This project also looks to improve our alignment with the guidance published by the International Medical Device Regulators Forum (IMDRF) and the regulatory approach of countries that are members of the MDSAP. 

In addition to the TGA, the MDSAP members include medical device regulators from Brazil, Canada, Japan and the United States of America (US). These are an increasing number of observer and affiliate regulatory authority members from other countries.

As an MDSAP member Australia will achieve the full benefits of this rapidly growing program by aligning, where possible, with other participating regulatory authorities.

Consultations