The Ministry of Health collects data to:
- monitor the health of New Zealanders
- manage subsidies and services
- inform funding and resource allocation
- determine and evaluate health services
- inform the development of health policies and interventions
- assist clinical decisions about patient care
- meet legislative requirements:
- New Zealand Public Health and Disability Act 2000 (external link)
- Health Act 1956 (external link)
- Privacy Act 2020 (external link)
- Health Information Privacy Code 2020 (external link)
- Health (Retention of Health Information) Regulations 1996 (external link)
- Official Information Act 1982 (external link)
- Cancer Registry Act 1993 (external link) and Cancer Registry Regulations 1994 (external link)
- Public Records Act 2005 (external link)
- meet international commitments, including:
- International Health Regulations 2005 (external link) (eg, death data is sent to the World Health Organization annually for international comparisons of mortality).