Simple Summary Cancer registration has a long tradition in Germany. In 2013, new
legislation obliged all German states to implement additional clinical cancer registration …

Aim To provide insight into cancer registration coverage, data access and use in Europe.
This contributes to data and infrastructure harmonisation and will foster a more prominent …

Population-based cancer registries are responsible for collecting incidence and survival
data on all reportable neoplasms within a defined geographical area. During the last …

Population-based cancer registries have a long-standing role in cancer monitoring.
Scientific use of cancer registry data is one important purpose of cancer registration, but use …

Abstract Background: The Nordic Cancer Registries are among the oldest population-based
registries in the world, with more than 60 years of complete coverage of what is now a …

Objectives To assess the quality of cancer registry in primary care. Design and setting A
cross-sectional validation study using linked data from primary care electronic health …

Today, many countries are increasing their efforts to ensure that all cancer patients receive
the best possible care. Population-based cancer registries have adapted their registration to …

Cancer registries (CR) are the fundamental source of objective cancer data, and thus are
indispensable for the evaluation of the cancer burden and for design of effective cancer …

Abstract Background In Scandinavia, there is a strong tradition for research and quality
monitoring based on registry data. In Denmark, Norway and Sweden, 63 clinical registries …

Currently about 160 population-based cancer registries (CRs) in Europe have extensive
experience in generating valid information on variation in cancer risk and survival with time …