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MAGIC: once upon a time in consent management—a FHIR(®) tale
BACKGROUND: The use of medical data for research purposes requires an informed consent of the patient that is compliant with the EU General Data Protection Regulation. In the context of multi-centre research initiatives and a multitude of clinical and epidemiological studies scalable and automatable...
Autores principales: | Bialke, Martin, Bahls, Thomas, Geidel, Lars, Rau, Henriette, Blumentritt, Arne, Pasewald, Sandra, Wolff, Robert, Steinmann, Jonas, Bronsch, Tobias, Bergh, Björn, Tremper, Galina, Lablans, Martin, Ückert, Frank, Lang, Stefan, Idris, Tarik, Hoffmann, Wolfgang |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6137912/ https://www.ncbi.nlm.nih.gov/pubmed/30217236 http://dx.doi.org/10.1186/s12967-018-1631-3 |
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