National health information platform

Better data, better access, better sharing, better health and wellbeing

A Ministry of Health team is working in partnership with consumers, the health and disability sector, and technology providers to deliver a national health information platform (nHIP).

A business case seeking support for the development of nHIP is being considered by Cabinet.

nHIP is an ecosystem of data and digital services that enable a whole new way for a person’s health information to be accessed and updated. It will transform the way people interact with health services and use their health information.

Consumers will be able to access and control their health information through their choice of website or application using a digital device such as a smartphone, tablet or computer. Change and adoption is a significant focus for the programme and we will also consider what options exist for people who don’t have access to, or prefer not to use, technology.

Better access to health information – anywhere, anytime

nHIP enables access to a virtual electronic health record as needed by drawing together a person’s latest health data from trusted sources to create that data.

nHIP is focused on:

  • Improving equity of access to health information and health services; to empower and support consumers and whānau to better manage their health and wellbeing; and improve the performance of the health system.
  • Providing access to data and digital services that make health information more accessible and interoperable, and result in better quality data for improved insights and decision-making.
  • Making it easy to use nHIP data and digital services so that they are adopted widely in the sector and support greater system and market innovation.

Consumers will have better access to their health information and can control who they share it with. Providers will have secure, easy access to patient information, in the right context and at the right time.

Improving Māori health outcomes is a priority. nHIP will target equity challenges and identify ways to address these. The principles of Māori data governance will be incorporated.

Why change is needed

  • Many of our health and disability information sources aren’t joined up, and there is variation in how data is collected and stored, and in its quality.
  • Data is not always accessible to help a person receive the best health care for their needs.
  • It is not easy for New Zealanders to access or control their own health information, or to share it with trusted family and whānau.

Consumers and whānau at the centre

  • Consumers and whānau must be at the centre of nHIP, so it works effectively and equitably for them.
  • Along with the Department of Internal Affairs, we have worked with over 70 consumers and whānau, and health professionals to really understand the challenges.
  • We learnt that these four key features should be prioritised in the project:
    • Delegation and authorising access – the ability to view, update and share information with permitted whānau and family
    • Customisable content to increase choice and control, allowing people to share the parts of their story they believe are most important
    • Wrap-around services to support the introduction and buy-in of new technology for consumers and health practitioners and improve the end-to-end health care experience
    • Establishing meaningful relationships within communities that will foster trust in the health care system for consumers and whānau.

nHIP tranche 1

Tranche 1 of nHIP runs to January 2024.

Tranche 1 will provide access for providers and consumers to important health information including demographics such as gender, ethnicity, name and date of birth; enrolled general practice; Community Service Card entitlements; prescribed and dispensed medicines; COVID-19 vaccination status and laboratory test results. As part of tranche 1, consumers will have the ability to update information held in the national health index (NHI), such as their contact details. Work is underway to enable people to update data on their iwi affiliations.

Access to health information in tranche 1 will be enabled through multiple consumer and provider channels (websites and apps), focusing on those that improve equity of access to health information and empower consumers and whānau to better manage their health and wellbeing.

Tranche 1 will also deliver technology enablers such as digital identity and interoperability services.

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