By coupling information from registries, researchers can obtain new knowledge of great value with regard to widespread medical conditions such as cardiovascular disease, cancer and depression. On the basis of registries, research results can be enhanced, as they draw on a larger population. Within social science, research on the basis of registries enables researchers to obtain essential knowledge about the long-term correlation of a number of social conditions such as unemployment and education with other life conditions. Research results obtained through registries provide solid, high-quality knowledge which can provide the basis for the formulation and implementation of knowledge-based policy, improve the quality of life for a number of people and improve the efficiency of social services. In order to facilitate scientific research, personal data can be processed for scientific research purposes, subject to appropriate conditions and safeguards set out in Union or Member State law.
GDPR Recital EN
Recital 157
Related across sources
Guidance Guidelines 05/2020 on consent under Regulation 2016/679 Guidance Guidelines 07/2020 on the concepts of controller and processor in the GDPR Guidance Guidelines 01/2022 on data subject rights - Right of access Guidance Version history Guidance Guidelines 01/2021 Guidance Guidelines 2/2018 on derogations of Article 49 under Regulation 2016/679