Clinical registries play an important role in improving healthcare by collecting and analysing patient outcomes. They help clinicians and services understand where care varies, compare performance and use these insights to improve care over time.
That’s why clinical registries are a key focus within the CEIH’s Priority Focus Area on data-driven clinical decision making. This reflects our commitment to improving how clinical registries are developed, connected and used across South Australia.
Across the series, speakers from South Australia and beyond shared practical clinical, data and governance insights, showing how well-designed registries are being used in real settings to support evidence-based decision making and continuous quality improvement.
Episode 59: Getting Clinical Registry Governance Right: Trust, Access and Use
Tamara Hooper (Strategic Director, SAHMRI Registry Centre)
Professor Andrew Bersten (Executive Director of Research, SALHN) and Karen Saxty (Director Research Operations, SALHN)
Strong governance is what turns registry data into safe, usable insight.
In this episode, learn about:
- the work of the South Australian Health and Medical Research Institute (SAHMRI) Registry Centre, outlining common governance challenges and showing how well-designed governance can support high-quality research, inform policy and drive continuous improvement in clinical care
- how the Southern Adelaide Local Health Network (SALHN) is moving from fragmented registry practices to a more consistent governance model, exploring challenges and lessons learned, including managing new and existing registries, system and platform variation, and consent and ethical considerations.