This webinar delves into how the National Cancer Screening Register supports the patient bowel screening journey and contributes to population health data and policy improvements. Learn about the benefits of the register, clinical software integration and delegations, and understand how to work with and report to the register. The webinar will also cover how to integrate the register into practice software, troubleshoot issues and find supporting resources.

Key topics include the importance of the National Cancer Screening Register in public health data, its role in bowel kit distribution and patient follow-up, and the interaction between the pathology provider and the register. Attendees will also explore the benefits of accessing the healthcare provider portal, updating patient details, and the significance of reporting. This comprehensive session aims to equip healthcare providers with the knowledge and tools to effectively utilise the National Cancer Screening Register for improved patient care and streamlined practice operations.

Learning Outcomes

At the completion of this webinar, you will be able to: 

Outcome 1: Identify how the National Cancer Screening Register supports the patient screening journey and contributes to population health data and policy improvements

Outcome 2: Determine the benefits of utilising the National Cancer Screening Register, including through clinical software integration and delegations

Outcome 3: Identify healthcare professionals’ roles and processes for working with and reporting to the National Cancer Screening Register.

Outcome 4: Identify resources and processes for integrating the National Cancer Screening Register into your practice software and how to troubleshoot issues

Presenter Information

Professor Vivienne Milch, Medical Director at Cancer Australia

As Medical Director of Cancer Australia, I provide strategic clinical policy oversight and leadership to Cancer Australia, and advice to the Commonwealth Department of Health and Aged Care on national cancer screening policy.

Cancer Australia was established by the Australian Government in 2006 to benefit all Australians affected by cancer, and their families and carers. Cancer Australia aims to reduce the impact of cancer, address disparities and improve outcomes for people affected by cancer by leading and coordinating national, evidence-based interventions across the continuum of care. Our work includes the translation of evidence into policy and practice to advance patient-centred care; innovative and sustainable models of best practice cancer care and investment in priority areas of cancer research.

I am passionate about the importance of early detection of cancer, equity of access to optimal cancer care, multidisciplinary survivorship care, and improving the lives of all Australians affected by cancer.

John Lee, Head of Engagement and Communication for the National Cancer Screening Register at Telstra Health

John Lee is a healthcare engagement and communications specialist with over a decade of experience in cancer screening, mental health promotion, and public health initiatives. He is currently the Head of Engagement and Communication for the National Cancer Screening Register t Telstra Health, where he focuses on improving participation in screening programs. Previously, he worked with SuperFriend and BreastScreen Victoria, leading recruitment campaigns and stakeholder partnerships.    

His career spans Australia and the UK, including roles in the NHS. With a background in marketing and public relations, John has developed large-scale communication strategies that enhance healthcare accessibility and awareness. His passion for preventative health continues to drive initiatives that improve outcomes for communities nationwide. 

CPD

Educational activities: 1 hour