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The use of health data for public health, surveillance, quality improvement and research is crucial to improve health systems and health care. However, bodies responsible for privacy and ethics often limit access to routinely collected health data. Ethical approvals, issues around protecting privacy and data access are often dealt with by different layers of regulations, making approval processes appear disjointed.

journal of innovation in health informatics

Using routinely collected health data for surveillance, quality improvement and research: Framework and key questions to assess ethics, privacy and data access