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Record linkage research and informed consent: who consents?
BACKGROUND: Linking computerized health insurance records with routinely collected survey data is becoming increasingly popular in health services research. However, if consent is not universal, the requirement of written informed consent may introduce a number of research biases. The participants o...
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| Hoofdauteurs: | , , , |
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| Formaat: | Artigo |
| Taal: | Inglês |
| Gepubliceerd in: |
BioMed Central
2007
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| Onderwerpen: | |
| Online toegang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC1802736/ https://ncbi.nlm.nih.gov/pubmed/17291357 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1472-6963-7-18 |
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