Ethical and legal constraints on data sharing between countries in multinational epidemiological studies in Europe report from a joint workshop of the European League Against Rheumatism standing committee on epidemiology with the "AutoCure" project.
expert_opinion · Level V
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- Record sourced from PubMed, PMID 18180280.
- Also identified by DOI 10.1136/ard.2007.080598.
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Abstract
We report on a workshop on ethical and legal constraints on data sharing between countries in multinational epidemiologic research in Europe that was held in January 2007 in Potsdam, Germany. The participants were experienced epidemiologic and clinical researchers from eight European countries. The aim of the workshop was to share current knowledge on the above-mentioned topics, to identify areas for joint action and to enhance the likelihood of success for the new funding programmes. Workshop sessions and review of findings. Key elements and recommendations have been drawn up. Epidemiologic and clinical studies are increasingly planned and conducted on a European level, and funds are available for this kind of studies. However, data sharing in multi-centre clinical and epidemiological studies is hampered by the different legal and ethical constraints individual national researchers face.
Medical subject headings
- Biomedical Research
- Ethics, Research
- International Cooperation
- Multicenter Studies as Topic
- Rheumatic Diseases