The main aim of JA:EHLEIS is (i) to provide a central facility for the co-ordinated analysis and synthesis of life and health expectancies to add the quality dimension to the quantity of life lived by the European populations, (ii) provide evidence of inequalities between Member States (MS) and (iii) highlight potential targets for public health strategies both nationally and at a pan-European level.
Two previous projects have been conducted to promote the Structural Indicator HLY, based on the development of an Information System and research work to monitor health trends and gaps in Europe.
During the first phase (2004-2007) the EHEMU project developed several summary measures of population health (SMPH) indicating the quality of the remaining years that a person is expected to live (i.e. free of chronic disease, free of disability and in good perceived health).
In the second phase (2007-2010) the EHLEIS project began to systematically monitor health trends and gaps among the European countries and to identify their determinants through the survey instruments developed by EHEMU and included in the new pan-European survey SILC (European Statistics on Incomes and Living Conditions) and SHARE (Survey on Health, Ageing and Retirement in Europe).

TEHDAS, the joint action Towards the European Health Data Space, helps EU member states and the European Commission to develop and promote concepts for the secondary use of health data to benefit public health and health research and innovation in Europe. Its goal is that in the future European citizens, communities and companies will benefit from secure and seamless access to health data regardless of where it is stored.

The Data Portal brings together and continuously updates the relevant COVID-19 datasets and tools.

An unprecedented number of scientific efforts are taking place worldwide in order to help combat the new coronavirus epidemic (COVID-19). One of the biggest challenges in this fast-moving situation is to share data and findings in a coordinated way, in order to understand the disease and to develop treatments and vaccines.

To address this challenge, EMBL-EBI and partners operate the COVID-19 Data Portal, which brings together relevant datasets submitted to EMBL-EBI and other major centres for biomedical data. Our aim is to facilitate data sharing and analysis, and to accelerate coronavirus research.

The COVID-19 Data Portal enables researchers to upload, access and analyse COVID-19 related reference data and specialist datasets.

The COVID-19 Data Portal is the primary entry point into the functions of a wider project, the European COVID-19 Data Platform.

The BeYond-COVID project aims to make COVID-19 data accessible to scientists in laboratories but also to anyone who can use it, such as medical staff in hospitals or government officials.

Going beyond SARS-CoV-2 data, the project will provide a framework for making data from other infectious diseases open and accessible to everyone.

Through country collaboration, InfAct streamlines health information activities across Europe. It builds towards a sustainable and solid infrastructure on EU health information and strengthens its core elements based on capacity building, health information tools and political support.

PHIRI is a roll-out of the research infrastructure on population health information to facilitate and generate the best available evidence for research on health and well-being of populations as impacted by COVID-19. PHIRI will allow for better coordinated European efforts across national and European stakeholders to generate the best COVID-19 population health knowledge. In doing so, PHIRI will lay the foundation to build a Distributed Infrastructure on Population Health (DIPoH) to be used to overcome future crisis and ensuring the sustainability of the project. The intent is to support research across Europe through the identification, access, assessment and reuse of population health and non-health data to underpin public health policy decisions. This will be achieved through a close collaboration with 41 partners across 30 countries over a period of 36 months starting in November 2020. The project is divided in 9 ambitious work packages with three transversal topics. PHIRI builds on the achievements of the BRIDGE Health and the Joint Action on Health Information (InfAct) projects.

To produce a revised set of reproductive health indicators for the enlarged EU; To construct a compendium of reproductive health data currently available within the EU; To develop standard operation procedures for the appropriate use of the reproductive health indicators throughout the EU; Develop and pilot a youth reproductive health survey for use by selected Member States. 
To assess the usefulness of a comprehensive set of sexual and reproductive health indicators designed for the enlarged European Union, with particular emphasis on the reproductive health of adolescents and young adults

To validate the potential of the Injury database IDB to fulfil the requirements of the European statistical system by integrating these data with the existing hospital discharge registers (HDRs). The overall goal is to develop and evaluate a data model for the integration of routine and more detailed hospital data on injuries, namely thru linking the official HDR with the EU-IDB.

To assist European, national, regional and local decision makers in developing their health policy, through a better understanding of the health status of the population and of health inequalities at regional and sub regional level