Medical devices reforms: low-risk products

Project overview

In response to the 2015 Expert Review of Medicines and Medical Devices Regulation, the TGA reformed the regulation of a number of low-risk products

Reform to the regulation of low-risk products is occurring two streams:

• Class 1 medical devices
• Other therapeutic goods and excluded goods

Further reforms to low-risk devices are under consideration.

Consultations

More information

• Consultations and reviews.