2. DHB/Region level
• Know are we doing the right thing, is it safe,
what patients want, effective.
• Need to know everything from population
health to individual outcomes for treatment.
• Need to facilitate open and transparent
information for patients, clinicians, organisations
and communities.
• To have confidence in the interpretation of data.
3. Comparative trusted information`
• Feels like hard work.
• Warehouse where everyone can dive in and get what
they want.
• Multiple analysis of data.
• Behind closed doors - what assumptions are being
made about the data?
• Judgements about quality ,completeness.
• Not transparent.
4. Trusted information
• Strategic view of information.
• Challenging the transparency agenda - do we believe in open data?
• Information governance, data quality timeliness completeness.
• Information standards.
• Transparent interpretation of data-confidence in the way it is being
used to transform decision making regulation and policy.
• Public confidence about the use of data and access to it.
• Maximisation of specialist skills, resources and expertise.
• Designing ways of accessing data that is not currently readily
available.
• Identifying levers and incentives to encourage best practice use of
information.