Prototypical clinical trial registry based on fast healthcare interoperability resources (FHIR): design and implementation study
- Language
-
Englisch
- Identifier
-
1307491782
Contributor
Gulden, Christian
Blasini, Romina
Nassirian, Azadeh
Stein, Alexandra
Altun, Fatma Betül
Kirchner, Melanie
Prokosch, Hans-Ulrich
Boeker, Martin
Blasini, Romina
Nassirian, Azadeh
Stein, Alexandra
Altun, Fatma Betül
Kirchner, Melanie
Prokosch, Hans-Ulrich
Boeker, Martin
- DOI
-
10.2196/20470
- URN
- Rights
-
Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Last update
-
07.12.2023, 3:21 PM CET
Associated
- Gulden, Christian
- Blasini, Romina
- Nassirian, Azadeh
- Stein, Alexandra
- Altun, Fatma Betül
- Kirchner, Melanie
- Prokosch, Hans-Ulrich
- Boeker, Martin
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Interviews with experts in rare diseases for the development of clinical decision support system software - a qualitative study
Integrating clinical decision support systems for pharmacogenomic testing into clinical routine - a scoping review of designs of user-system interactions in recent system development
Evaluation of a clinical decision support system for rare diseases: a qualitative study
Prototypical Clinical Trial Registry Based on Fast Healthcare Interoperability Resources (FHIR): Design and Implementation Study
Patient recruitment system for clinical trials: mixed methods study about requirements at ten university hospitals
The architecture of a feasibility query portal for distributed COVID-19 fast healthcare interoperability resources (FHIR) patient data repositories: design and implementation study
Applied Practice and Possible Leverage Points for Information Technology Support for Patient Screening in Clinical Trials: Qualitative Study
Interviews with experts in rare diseases for the development of clinical decision support system software - a qualitative study
Visualization of similar patients in a clinical decision support system for rare diseases – a focus group study
Interviews with experts in rare diseases for the development of clinical decision support system software - a qualitative study
Implementing pharmacogenomic clinical decision support into German hospitals
A nationwide registry for recurrent urolithiasis in the upper urinary tract – The RECUR study protocol
Interviews with experts in rare diseases for the development of clinical decision support system software - a qualitative study
Integrating clinical decision support systems for pharmacogenomic testing into clinical routine - a scoping review of designs of user-system interactions in recent system development