Agent access to notifications on Post Market Review Medical Devices Compliance dashboard

Overview

From 19 October 2020, the process by which the Therapeutic Goods Administration (TGA) engages with sponsors changed. A new medical device Post Market Review Compliance Dashboard  was developed in TBS to respond to post market reviews. The new compliance dashboard provides sponsors with an efficient and secure way of responding to post market reviews.

At present, the Post Market Review Medical Devices Compliance portal does not grant access to authorised agents of sponsors. The purpose of the survey was to seek input regarding the preferred way for granting access to authorised agents.

What happens next

Responses have been collated and will be used for guiding the TGA in improving the Post Market Review Devices Compliance dashboard.