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We welcome offers to develop our collection that relate to the history of the College and child health. Our Archive Collection Policy defines our archival collections and gives information about what we accept.

Since 2014, we've invited stakeholders from across the rare disease community to this informal networking event. Young people speak about their experiences of living with a rare disease, and patient advocates, researchers and health professionals talk about working in the field. Read on for highligh...

On 12 November 2020, the National Neonatal Audit Programme (NNAP) hosted its inaugural virtual update event as a live webinar. You can access resources from the event on this page.

The National Neonatal Audit Programme (NNAP) and Neonatal Data Analysis Unit (NDAU) Collaborators' meetings are a great opportunity to network and learn more about how data is being used to monitor and improve neonatal care. Take a look at this year's presentations.