The New Zealand Children’s Cancer Registry (NZCCR) is a population-based registry which holds verified demographic and treatment information for all children diagnosed with cancer in New Zealand since January 2000. This data is used to guide clinical practice, inform child cancer service planning and for evaluating health outcomes for children with cancer in New Zealand.
The NZCCR Working Group is responsible for the ongoing co-ordination and analysis of this registry. Their responsibilities include:
For more information contact:
Gemma Pugh, NCCN Research Lead