Good morning fellow OMOPers!
I’m involved in a project that wants to leverage the use of real world data from European and other international Multiple Sclerosis registries by transforming the data to OMOP CDM.
Since the registries are heterogeneous in their data (data types, format, export files, variables etc.), this is a huge task to tackle. One reason to go with the OHDSI approach was the big, supportive community behind it. That’s why I’m reaching out to you now.
I’m looking for fellow data scientists, researcher, developer, doctors, nurses, students - whoever! - who would like to form a work group concerning registry data and its transformation to OMOP CDM. The use case of the registry is not important.
Feel free to contact me, if you’re interested!