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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...
| Autores principales: | , , , , , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
Springer International Publishing
2020
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| Materias: | |
| 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 |