A hospital contacted us with the challenge of automating the analysis of the research information from clinical trials to reduce the time researchers spent in the analysis. We developed a platform to do this through pre-designed or customized templates. These templates have the following characteristics:
– Customized: through the collection of information about the study or trial, the configuration of the analysis according to the researcher criteria, the definition of the goals and outputs of the analysis and the setting of variables, naming and standards to be used.
– Pre-designed/Shared: the platform allows the sharing of templates with other users or teams to be used in other similar studies. For example, a medical study can be reproduced in another country/medical Centre using the exiting template and providing the new data.

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