The National Cancer Screening Register (the Register) is a national electronic infrastructure for the collection, storage, analysis and reporting of screening program data for the renewed National Cervical Screening Program. 

In December 2017 the Register went live and became functional to accept cervical screening results from pathology labs in Australia.

In 2018 the Register will create a single national record for participants of the new National Cervical Screening Program following transition from the current state-based registers. It will also eventually replace the existing National Bowel Cancer Screening Register and create a single national record for participants of the National Bowel Cancer Screening Program.

The Register will provide ongoing clinical service delivery data to appropriate health professionals to support quality improvement and service delivery.

Why the need for a national Register

  • Each year almost 900 people are diagnosed with cervical cancer. The need to build Australia’s capacity to screen for this cancer is a national priority.
  • The Register optimises screening for, and preventing, cervical cancer by capturing a single electronic record for each person in Australia participating in cervical screening. We use invitations to screen, reminders when screening is overdue, and follow up of adverse results, to support prevention and early detection of cervical cancer.
  • The Register is a leading digital health service that holds nationally consistent health information in a central location, while allowing electronic access to this information to support timely clinical decisions.
  • We will provide a high quality, safe and cost-effective health service to help prevent cervical cancer.

How will the Register support the National Cervical Screening Program?

We will support the National Cervical Screening Program by: 

  • Maintaining a national database of cervical screening records 
  • Inviting eligible persons to commence cervical screening when they turn 25 years
  • Reminding participants when they are due and overdue for cervical screening
  • Providing a participant’s cervical screening history to laboratories to inform screening recommendations
  • Providing a ‘safety net’ for participants who are at risk and who have not attended further testing, by prompting them to have follow up tests
  • Enhancing strict data security – data collected by the Register is protected by legislation and is maintained under the National Cancer Screening Register Act 2016 and other relevant laws.