Abstract
Abstract In order to transfer data from individual IVF centers and a national register into a regional register and then merge this data into a world register, certain basic definitions must be established. The treatment strategies of each country are influenced by the legislative and insurance framework. The expectations of patient couples also vary greatly from region to region. All of this can only work if there are definitions of what data is to be collected and in what way. Above all, there are difficulties in creating statistics when the raw data first has to be adjusted and merged. This article is intended to point out some difficulties, but also to show solution concepts.
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