TGA's New Post Market Review Compliance Dashboard

Closed 31 Dec 2021

Opened 8 Nov 2020

Contact

1800 141 144

devices@tga.gov.au

Feedback updated 18 Sep 2025

We asked

The respondents were asked to use the TGA’s Post Market Review Compliance Dashboard and provide feedback about its efficiency and security. These questions included the following topics:

  • navigation,
  • how intuitive the system was,
  • viewing and submitting notifications,
  • data entry,
  • uploading documents, and
  • requesting extensions.

You said

We received 10 submissions in response to the survey. Eight submitters provided permission for their responses to be published on the TGA website. These are available through the ‘View submitted responses’ link below. Generally, respondents found that while the system was relatively easy to use, there were some areas that could be improved. There were also some parts of the system that were not reviewed by respondents.

We did

The feedback provided by respondents has been collated and will be included in future changes to the system.

Results updated 18 Sep 2025

Only answers from respondents who gave permission are published. However, all responses are included in the analysis of this activity.

Respondents were invited to complete the survey on the New Post Market Review Compliance Dashboard. The submissions are now available below.

8 Published responses

ANON-VVFN-YP1D-X

RIDGEBACK LOGISTICS_Peter Damian Turner

ANON-VVFN-YP1A-U

R&H Imports_Raghu Yerrasani

ANON-VVFN-YP1Y-K

ANON-VVFN-YP1H-2

IST Australia Pty Ltd

Henry Schein

Files:

Overview

From 19 October 2020, how the TGA engages with the sponsors for post market reviews has changed. A new medical device Post Market Review Compliance Dashboard  has been developed in TBS to respond to post market reviews. The new compliance dashboard will provide the sponsors with an efficient and secure way of responding to post market reviews.

The purpose of this survey is to seek your feedback on the new Post Market Review Compliance Dashboard. 

Why your views matter

In the TGA's new medical device  Post Market Review Compliance Dashboard, the sponsors will be able to directly respond to post market reviews. The sponsors will receive regulatory requests for information via email and directed to the dashboard through TBS in which they will find new requests for information, submitted requests for information and any requests for information that they have saved but not yet submitted. The sponsors will also be able to upload and submit large files for the post market reviews. Therefore reducing the need to send in information on USB or CD’s and eliminating the risk of these devices getting lost or not being received. 

We invite you to provide your feedback on the new Post Market Review Compliance Dashboard by completing our online survey (click on the link below).

What happens next

Submissions will be reviewed by the TGA. A summary of responses will be published and all submissions will be placed on this website (unless marked confidential or indicated otherwise in the survey or submission form).

Outcomes from the consultation will be provided to the Government for consideration.

Audiences

  • Medical Devices & IVDs
  • Other