Report Results on the High Value Data Collections Survey

Report Results on the High Value Data Collections Survey

Monday, October 30, 2017

Report Results on the High Value Data Collections Survey

As part of our commitment to service improvement, the Population Health Research Network (PHRN) conducted a project about identifying and prioritising high value data collections for linkage.

The primary aim of the project was to identify an agreed minimum set of data collections to be consistently included in each of the PHRN nodes data linkage infrastructure in order to support projects conducted at national or multi-jurisdictional levels.

Thank you to the nearly 300 people who participated in the survey.

The project started on 1 January 2017 and was completed by 30 June 2017.   The results of the report are attached here.


For more information contact the PHRN.

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PHRN COVID-19 Offering

Our network remains open. The network is interoperable & can source expertise, technology & data from around the country. Our expert staff are highly qualified & experienced in linkage of patient data, including population-based administrative data as well as linkage of research cohort data.

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PHRN National Researcher Training Project: Stakeholder Survey PHRN is undertaking a survey about data linkage and communications. We wish to invite you to participate. This survey is part of the PHRN National Researcher Training Project (phase one).