Secondary research use of personal medical data: attitudes from patient and population surveys in The Netherlands and Germany

Making routine clinical-care-data available for medical research requires adequate consent to legitimize use and exchange. While, public interest in supporting medical research is increasing, individuals often find it difficult to actively enable researchers to access their data. In addition to broa...

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Detalles Bibliográficos
Autores principales: Richter, Gesine, Borzikowsky, Christoph, Lesch, Wiebke, Semler, Sebastian C., Bunnik, Eline M., Buyx, Alena, Krawczak, Michael
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer International Publishing 2020
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7940390/
https://www.ncbi.nlm.nih.gov/pubmed/33005018
http://dx.doi.org/10.1038/s41431-020-00735-3

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7940390/
https://www.ncbi.nlm.nih.gov/pubmed/33005018
http://dx.doi.org/10.1038/s41431-020-00735-3

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