The Dutch Cancer Atlas, launched in January 2023 by the Netherlands Comprehensive Cancer Organisation (IKNL) is now available also in English.
The interactive online atlas shows geographical patterns… more
The new Quality Check Software Kit is now available for download. It includes the new QCS 2.1 and the latest version of the CVS Data Layout Converter, the tool used to check the compatibility of the incidence file format with the QCS according to the latest ENCR-… more
This User Insights Survey is part of the… more
The Organisation
The National Cancer Registry is an essential part of Ireland’s efforts to successfully control cancer, reducing its impact on individuals, families and society.
The National Cancer Registry (“NCRI”) was established by the Minister for Health in 1991 by Statutory Instrument and is… more
The 2022 cancer incidence and mortality estimates for EU-27 and European countries have been published in the European Cancer Information System (ECIS) at… more
The European Commission Joint Research Centre (JRC), the ENCR and EUROCARE organised a training on basic statistical analysis of cancer registry data European Commission Joint Research Centre in Ispra, Italy.
The training on data coding, was organised jointly by the ENCR Steering Committee and the European Commission Joint Research Centre. The aim was to improve comparability and harmonisation, particularly on coding topography/morphology and stage.
JRC and ENCR organised on 3-4 May 2017 a training on Cancer Data Collection and Comparability with one day devoted to issues related to data collection, and the second day to quality aspects of data analysis. A specific session on childhood cancer registration was included.
The Paediatric Oncology for Cancer Registries is a unique course, organized by the International Agency for Research on Cancer (IARC) in the framework of the European Network for Cancer Research in Children and Adolescents (ENCCA), a Network of Excellence funded by the European Commission in FP7.… more
The aim of the training is to provide cancer registries staff with an understanding of good practices and procedures to establish/improve their registries and harmonise their process for collection of cancer data. This will facilitate inter-comparative studies on specific cancer types which in turn… more
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