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Get Data Out – the impact of cancer data

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How to make data on small groups of cancer patients accessible, safe and clinically relevant

About this event

Hosted by the National Disease Registration Service (NDRS) and Cancer52, this webinar will explore:

• What is the impact of routinely publishing anonymised patient data on detailed statistics, including incidence, routes to diagnosis, treatment and survival, particularly for rare and less common cancers?

• How have stakeholders have utilised data from the Get Data Out Programme?

Speakers:

1. Anna Cooper, Cancer Information Analyst, NDRS

2. Charlotte Eversfield, Senior Cancer Intelligence Analyst, NDRS

3. Thomas Harding, Knowledge Officer, Prostate Cancer UK

4. Lydia Makaroff, Chief Executive, Fight Bladder Cancer

5. Alan Moss, Action Against Heartburn

6. Helen Bulbeck, Director of Policy and Services, Brainstrust

7. Georgia Papacleovoulou, Senior Policy and Intelligence Manager, Pancreatic Cancer UK

This webinar is open to the public, although it may be more useful for those working in healthcare, commissioning, public health, policy or for a cancer alliance or charity.

The webinar will be hosted on MS Teams and it will be recorded and uploaded to the NDRS website shortly after. There will be time for Q&A at the end of the talk.

You will be sent joining instructions for this webinar 2 days beforehand.

***PLEASE CHECK YOUR JUNK FOLDER FOR THE EMAIL FROM EVENTBRITE WITH THE LINK TO JOIN***

If you have any questions about this webinar or registering to attend, please contact NDRSengagement@phe.gov.uk.

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Organiser National Disease Registration Service (NDRS)

Organiser of Get Data Out – the impact of cancer data

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