MAGIC: once upon a time in consent management$da FHIR® tale
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 measures fo...
Gespeichert in:
| Hauptverfasser: | , , , |
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| Dokumenttyp: | Article (Journal) |
| Sprache: | Englisch |
| Veröffentlicht: |
14 September 2018
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| In: |
Journal of translational medicine
Year: 2018, Jahrgang: 16, Pages: 1-11 |
| ISSN: | 1479-5876 |
| DOI: | 10.1186/s12967-018-1631-3 |
| Online-Zugang: | Verlag, Volltext: http://dx.doi.org/10.1186/s12967-018-1631-3 Verlag, Volltext: https://doi.org/10.1186/s12967-018-1631-3 
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| Verfasserangaben: | Martin Bialke, Thomas Bahls, Lars Geidel, Henriette Rau, Arne Blumentritt, Sandra Pasewald, Robert Wolff, Jonas Steinmann, Tobias Bronsch, Björn Bergh, Galina Tremper, Martin Lablans, Frank Ückert, Stefan Lang, Tarik Idris and Wolfgang Hoffmann |
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| 520 | |a 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 measures for digital consent management are required. Modular form, structure, and contents render a patient’s consent reusable for varying project settings in order to effectively manage and minimise organisational and technical efforts. | ||
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