Webinar: Driving more equitable real-world evidence with CPRD

Delivered by the Medicines and Healthcare products Regulatory Agency (MHRA), the Clinical Practice Research Datalink (CPRD) is a world-leading research resource that has been empowering researchers with data-driven insights for more than 30 years. Its new Ethnicity Records are a step closer to more inclusive public health research and clinical practice.

Discover more at our next Data Access and Discovery Webinar!

  • When: Thursday 19 October
  • Where: Online
  • Time: 14:00 – 14:45

We’ll be joined by Eleanor Axson, Senior Researcher at CPRD-MHRA, who’ll take us on an in-depth tour of CPRD’s data service and its new Ethnicity Records.

Paola Quattroni, Head of Alliance Strategy and Engagement at HDR UK, will also provide an update on the UK Health Data Research Alliance’s Diversity in Data workstream, which brings together groups across the research community to discuss recommendations for improving the completeness, consistency and representativeness of routinely collected health and health-related data.

Open to anyone interested in understanding more about the use primary care data for public health research. Followed by a Q&A with additional panel members:

  • Ashley Akbari, Associate Professor of Population Data Science Research at Swansea University and Co-Chair of the Alliance Diversity in Data special interest group on ethnicity coding standards.
  • Mike McMillan, Business Development Team Leader at CPRD.

Register now to secure your spot at the next Data Access and Discovery Webinar!

Click here to register

Background reading: How CPRD is driving more equitable research