The aim of our review is to uncover which real world datasets, based on patient / disease based registries, exist in Europe regarding rheumatoid arthritis . We also aim to understand how these differ in the ability to conduct outcomes research using the available data.
In our initial research, we are attempting to answer the following question:
What is the impact of the journal articles related to the specific registries?
*Impact was calculated based on citation impact analysis for each identified article (for the last 10 years).
This is a summary of the top ten most frequent journals
We are currently in process to add data for additional registries regarding rheumatoid arthritis and will amend the blog-post as they become available.
Learn more about “Where is the best quality real world data set in Europe“ by clicking on the tag below.
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