Establish a sustainable network for researchers, funders, policy makers, advocates and young people in Europe, to support collaboration in developing the future of child health research.

Reitox directly contributes to the EMCDDA’s core task of collecting and reporting consistent, harmonised and standardised information on the drug phenomenon across Europe

The overall aim of the RECAP preterm Project is to improve the health, development and quality of life of these children and adults by developing the RECAP preterm Cohort Platform, a sustainable, geographically diverse and multidisciplinary database of national and European cohorts of babies born very preterm or with very low birth weight (VPT/ VLBW cohorts).

Understand the scale, relevance and directions of health professional mobility, the reasons behind it and the tools most adequate to respond to it; what impact does the movement of health professionals between European countries have on health systems?

Develop new standardised, harmonised and validated methods and tools for the assessment of costs and outcomes in European healthcare systems

To improve health by empowering a community to collaboratively generate the evidence that promotes better health decisions and better care.

MURINET aimed to create a European pool of experts in health and disability research and management, able to integrate several skills, within the framework of the ICF model.

MORGAM harmonizes data from population cohort studies from different countries and organizes genotyping and biomarker measurement in order to study the relationships between cardiovascular disease and risk factors.

To establish a large European cohort study of CHD and stroke in men and in women in all centres with follow-up data in the MONICA Project. To assess the predictive ability of the genetic polymorphisms of candidate genes for the subsequent development of CHD or stroke. The MONICA Project was established in the early 1980s in many Centres around the world to MONItor trends in Cardiovascular diseases (coronary heart disease (CHD) event registration is obligatory, stroke registration optional), and tolerate these to risk factor changes in the population over a ten year period.
To provide a scientific dissemination facility of the MONICA database in the form of CD files of data and also as a Monograph.