Reporting Guidelines

Reporting Guidelines

REporting of studies Conducted using Observational Routinely-collected Data (RECORD) is an international collaborative which has developed reporting guidelines for studies conducted using routinely-collected health data.

The aim of the collaborative is to enhance transparency by providing researchers with the minimum reporting requirements needed to adequately convey the methods and results of their research. The guidelines will also assist journals editors and peer reviewers critically assess manuscripts for publication.

Checklists are available for observational studies using routinely collected linked data and non-interventional pharmacoepidemiological studies using routinely collected health data. Other publications of interest include:

 

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HPV VACCINE

CASE STUDY

Data linkage has a significant role in reduction of cervical cancer in Australia. The HPV vaccine was introduced in 2007, success of the vaccine was monitored by linking vaccine registers to cervical smear registers in Queensland & Victoria.

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NEWS & EVENTS

LATEST NEWS

Read IJPDS' special issue on population data centre profiles featuring PHRN. With articles from population data centres across the world, this special issue represents a unique resource, bringing together into one place a wealth of information.

From 20 December 2019 the PHRN OAS will not be monitored. Normal operations will resume on 6 January 2020.

PHRN ONLINE APPLICATION SYSTEM (OAS)