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    • How data is kept safe and used responsibly
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    • Newsletter
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Menu
  • About us
    • Our work
    • Get Data Out
    • Our Partners
  • Patients
    • How data is collected
    • How data is kept safe
    • How data is used
    • Opt-out of disease registration
    • Genetic Enquiries
    • Your rights and privacy
  • Clinicians
    • What data is collected
    • How data is kept safe and used responsibly
    • The intelligence being provided
  • Data Stories
  • Resources
    • National Cancer Registration guide
    • Patient Leaflets
    • Trust Guidance
    • The NHS Cancer Quality of Life Survey
    • Publications
    • FAQs
    • Accessibility statement
  • News
    • Newsletter
    • Events
  • Blog
  • Get in touch

Resources

The National Cancer Registration and Analysis Service (NCRAS) has produced several resources to increase awareness of cancer registration with patients, the public and healthcare professionals. 

Click the links below to find out more.

National Cancer Registration guide

Patient Leaflets

Trust Guidance

The NHS Cancer Quality of Life Survey

Event Resources

Publications

FAQs

Newsletters

News and views

Access to NDRS data

Events

Get Data Out webinar – October 2021

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