SeeTreat Accessibility Statement

Accessibility statement for ART.1 Medical Device:

This accessibility statement applies to the ART.1 software as medical device accessible to users via web browser. ART.1 is manufactured by SeeTreat Pty Ltd. SeeTreat want as many people as possible to be able to use its products. AbilityNet has advice on making your device easier to use if you have a disability.

SeeTreat's ART.1 medical device is partially compliant with international Web Content Accessibility Guidelines (WCAG) 2.1 level AA compliance.

How Accessible this Medical Device is:

SeeTreat acknowledges some parts of the ART.1 medical device are not fully accessible:

• you cannot zoom to 400% without losing functionality
• you cannot adjust text spacing without relevant browser extensions
• pop-ups that are used on hover are not dismissible without moving pointer hover
• all functionality is not operable with a keyboard only
• the location of keyboard focus is not always visually obvious
• the are some restrictions on the focus indicator
• the focus indicator does not always have a clear thickness and indicator
• click and drag functions do not always have a non-mouse alternative
• when an error occurs, the issue is not always identifiable and described to the user in text
• appropriate labels or instructions are not always provided when content requires user input
• error messages are not always useful

Feedback and contact information

If you find any problems not listed on this page or think we're not meeting accessibility requirements, contact: support@seetreatmedical.com If you need information on this medical device in a different format like accessible PDF, large print, easy read, audio recording or braille:

• email support@seetreatmedical.com
• call +61 413 142 856

We'll consider your request and get back to you in 5 business days.

Enforcement procedure

The Equality and Human Rights Commission (EHRC) is responsible for enforcing the Public Sector Bodies (Websites and Mobile Applications) (No. 2) Accessibility Regulations 2018 (the 'accessibility regulations'). If you're not happy with how we respond to your complaint, contact the Equality Advisory and Support Service (EASS).

Technical information about this product's accessibility

SeeTreat is committed to making its website accessible, in accordance with the Public Sector Bodies (Websites and Mobile Applications) (No. 2) Accessibility Regulations 2018.

Compliance status

The ART.1 medical device has been tested against the Web Content Accessibility Guidelines (WCAG) 2.2 AA standard. The ART.1 medical device is partially compliant with the Web Content Accessibility Guidelines version 2.2 AA standard, due to the reasons listed in the above section “How Accessible this Medical Device is” listed below.

What SeeTreat is doing to improve accessibility

SeeTreat is committed to the continued improvement of accessibility to our products and are working towards improving accessibility to the items listed in the above section “How Accessible this Medical Device is” listed below.

Preparation of this accessibility statement

This statement was prepared on 15/08/2025. It was last reviewed on 15/08/2025. ART.1 was last tested on 12/08/2025 against the WCAG 2.2 AA standard. The test was carried out by SeeTreat Pty Ltd. You can read the full accessibility test report NHS Accessibility Criteria_SeeTreat internal test.xlsx.