Related Experiment Video
Updated: Oct 12, 2025

Drug Repurposing Hypothesis Generation Using the "RE:fine Drugs" System
Published on: December 11, 2016
Transfer of Clinical Drug Data to a Research Infrastructure on OMOP - A FAIR Concept
Ines Reinecke1, Michéle Zoch1, Markus Wilhelm1
1Institute for Medical Informatics and Biometry at Carl Gustav Carus Faculty of Medicine at Technische Universität Dresden, Germany.
Abstract:
Generating evidence based on real-world data is gaining importance in research not least since the COVID-19 pandemic. The Common Data Model of Observational Medical Outcomes Partnership (OMOP) is a research infrastructure that implements FAIR principles. Although the transfer of German claim data to OMOP is already implemented, drug data is an open issue. This paper provides a concept to prepare electronic health record (EHR) drug data for the transfer to OMOP based on requirements analysis and descriptive statistics for profiling EHR data developed by an interdisciplinary team and also covers data quality issues. The concept not only ensures FAIR principles for research, but provides the foundation for German drug data to OMOP transfer.
More Related Videos
Related Concept Videos
Clinical Trials: Overview
Clinically Relevant Drug Product Specifications: Methods of Establishment
Bioequivalence: Overview
Clinical Trials
There are four phases in a clinical trial. A phase one...
Bioequivalence studies: Biowaivers
Preclinical Development: Overview

