Swedish guidelines for registry-based randomized clinical trials

During the last decade Sweden has invested in a national infrastructure for collection of structured clinical data in the form of healthcare registries (in Sweden known as Kvalitetsregister). These data can be combined with other public data using the national personal identifiers that are issued to...

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Bibliographic Details
Main Authors: Karl Nyberg, Peter Hedman
Format: Article
Language:English
Published: Upsala Medical Society 2019-01-01
Series:Upsala Journal of Medical Sciences
Subjects:
Online Access:http://dx.doi.org/10.1080/03009734.2018.1550453