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All consortia are represented in the corresponding National Steering Committee, with the aim of aligning activities and agreeing parameters. Concept papers, defined requirements, and template texts will be jointly prepared and discussed in dedicated working groups, and consented by the National…

Intensive care medicine is an area of medicine in which a vast amount of data is collected digitally. However, a systematic, digital evaluation of this data to gain new scientific knowledge about specific diseases has not been done. The use of artificial intelligence in this data has enormous…

Any treatment with antibiotics can lead to pathogens developing resistance. Targeted use of antibiotics is therefore essential to avoid overtreatment and undertreatment. At the same time, bloodstream infections, including sepsis, are a widespread problem in hospitals, with the adequate use of…

Through the Medical Informatics Initiative (MII) and the establishment of Data Integration Centers, clinical care data from multiple sources in the Hospital Information System (HIS) are being made available for medical research. The result is a unique and rich pool of clinical data that is…

The Dialogue Forum allows representatives from the various groups to exchange ideas and information. Participants include patient advocacy groups, policy makers, government agencies funding organisations, research centres and other scientific institutions, and healthcare IT industry organisations…

The consent working group focuses on the design of the consent declaration signed by patients to allow healthcare data to be used in future medical research.

International planning workshop on 26 October 2020

New software makes FHIR resources accessible for statistical software

The data sharing working group is developing a legally robust framework for data access and usage within the scope of the Medical Informatics Initiative.