EUROCAT - European Surveillance of Congenital Anomalies

Search Open Yearbook

This information is part of the Open Yearbook, a free service of UIA's subscription-based Yearbook of International Organizations (YBIO). It includes profiles of non-profit organizations working worldwide in all fields of activity. The information contained in the profiles and search functionality of this free service are limited.

The full-featured Yearbook of International Organizations (YBIO) includes over 72,500 organization profiles, additional information in the profiles, sophisticated search functionality and data export. For more information about YBIO, please click here or contact us.

The UIA is a leading provider of information about international non-profit organizations. The aim of the Open Yearbook is to promote the activities of international non-governmental organizations (INGOs) and intergovernmental organizations (IGOs).

Contact Details

URL: https://eu-rd-platform.jrc.ec.europa.eu/eurocat_en

More detailed data available with paid subscription.

Founded

1979

History

Founded by DG-XII 'Science and Technology' of E-XE2442 - European Commission (EC), following 1975-1976 feasibility studies. 1991, status changed from research project to surveillance service under the coordination of DG-V 'Employment, Industrial Relations and Social Affairs, Health and Safety'. Evolved as a network of population-based registries for surveillance of congenital anomalies in Europe, which surveys about 25% of the European births. Central Registry, including central database, initially located at the Catholic University of Louvain (Belgium), then at the Scientific Institute for Public Health in Brussels (Belgium), subsequently at the London School of Hygiene and Tropical Medicine (UK), and finally at the University of Ulster, Northern Ireland (UK). 2015, Central Registry and European-level coordination activities of EUROCAT network transferred to the EC's Joint Research Centre (JRC), as an objective of the Administrative Arrangements (AA) signed by JRC and DG SANTE to implement EC's strategy in the field of rare diseases.

Aims

Provide essential epidemiologic information on congenital anomalies in Europe; facilitate early warning of teratogenic exposures; evaluate effectiveness of primary prevention; assess impact of developments in prenatal screening; act as an information and resource centre regarding clusters, exposures or risk factors of concern; provide a ready collaborative network and infrastructure for research related to causes and prevention of congenital anomalies and treatment and care of affected children; act as a catalyst for the setting up of registries throughout Europe collecting comparable, standardized data.

Events

22 past events available with paid subscription only.

Activities

Available with paid subscription only.

Structure

Annual Registry Leaders Meeting; Management Committee; Working Groups.

Languages

Available with paid subscription only.

Staff

Available with paid subscription only.

Finance

Available with paid subscription only.

Relations with Non-Governmental Organizations

Available with paid subscription only.

Publications

Available with paid subscription only.

Members

Available with paid subscription only.

Type I Classification

Available with paid subscription only.

Subjects *

Available with paid subscription only.

UN Sustainable Development Goals **

GOAL 3: Good Health and Well-being

UIA Org ID

XD1298

Last News

2021

* Subject classification is derived from the organization names and aims.
** UN SDGs are linked to the subject classification.

You are viewing profile from the Yearbook of International Organizations Online.
← return to your search page to find additional profiles.
Terms of Use

UIA allows users to access and make use of the information contained in its Databases for the user’s internal use and evaluation purposes only. A user may not re-package, compile, re-distribute or re-use any or all of the UIA Databases or the data* contained therein without prior permission from the UIA.

Data from database resources may not be extracted or downloaded in bulk using automated scripts or other external software tools not provided within the database resources themselves. If your research project or use of a database resource will involve the extraction of large amounts of text or data from a database resource, please contact us for a customized solution.

UIA reserves the right to block access for abusive use of the Database.

* Data shall mean any data and information available in the Database including but not limited to: raw data, numbers, images, names and contact information, logos, text, keywords, and links.