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...

Descripción completa

Detalles Bibliográficos
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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2018
Materias:
Methodology
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

Internet

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

Ejemplares similares