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...
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.