Get in touch with EOSC-Life

    COVID-19-related resources from EOSC-Life

    During a pandemic there is a need for timely and accurate collection, reporting and sharing of Individual Participant Data (IPD) from clinical trials. IPD should be stored in trustworthy data repositories that have been certified, are subject to rigorous governance, committed to longer-term preservation of their data and compliant with the relevant regulations (e.g. GDPR). This will facilitate reanalyses, secondary analyses and patient-level data meta-analyses. With the help of EOSC-Life, our partners are currently developing such a repository using the TSD platform for sensitive data. The repository will be part of the European COVID-19 Data Portal.

    Extension of the COVID-19 Data Portal The COVID-19 Data Portal brings together relevant datasets submitted to major centres for biomedical data, with the aim to facilitate data sharing and analysis, and to accelerate coronavirus research. Within EOSC-Life the COVID-19 Data Portal is extended to mobilise open biomolecular data (500,000 records from the biomolecular and literature domains are available openly to users), to mobilise new SARS-CoV-2 data (currently >160,000 viral isolates with raw sequence data; 75% of the world’s data flows through the Data Hubs) and to connect to clinical and epidemiological data.

    Due to the COVID-19 pandemic, the focus shifted towards providing tools and workflows to tackle analyses of COVID-related data in an open and reproducible way. The WorkflowHub was accelerated by 6 months and released early to provide a registry for COVID-19 workflows. In collaboration with the global Galaxy community, workflows have been made available on public Galaxy instances worldwide. 

    Our Training Open Calls offer funding to support training activities and provides expertise and guidance to help awardees organise successful and impactful training. Examples of funded projects are training and mentoring for Open Life Science Ambassadors, COVID-19 modelling, and cross-cluster training on modelling workflows with FATES for improving climate models.

      • Teaching researchers and clinicians how to share COVID-19-related data and software: The webinar & tutorial series is aimed at raising awareness in researchers, clinicians, and technicians who produce data and develop or use software related to COVID-19 about the outstanding importance of sharing data and software rapidly and openly. (no dates yet)
      • Training: Modelling COVID-19 Epidemics 
    • FAIRsharing EOSC-Life Collection 

    A collection of 100 diverse data resources (each containing thousands of datasets) following FAIR principles, produced by EOSC-Life partners.


    EOSC-Life believes that connecting digital life science data will transform our societies and allow us to address major challenges facing humanity, now including COVID-19

    To support the global effort to tackle the coronavirus pandemic, the Life Sciences Research Infrastructures (LS RIs) involved in EOSC-Life have been prioritising COVID-19 research, as detailed in the actions below. The benefits of using established Research Infrastructures are clear: they are ready and able to provide expert advice and resources to meet a variety of research needs. Although in-person visits to facilities may be restricted, many infrastructure services are still available via remote access and, where possible, the cost of access will be minimised or waived.

    Please follow the links provided by each LS RI for more information and to request access to their services.

    The video on the right presents 10 services of the European Life Science Research Infrastructures that can be used to advance research on coronavirus and other diseases.

    Samples, clinical data from biobanks & resources on standards


    The Research Infrastructure for biobanking and biomolecular resources has a network of over 600 biobanks across Europe, which can provide key services to researchers, such as:

    • Efficient and high-quality storage of samples in clinical and research settings;
    • Samples from healthy individuals, to be used as control (collected 2-3 months before outbreak in each country);
    • Guidance and standards for targeted identification, collection and conservation of important samples.

    Read more and download the document here.

    Rapid testing of binders/inhibitors to viral proteins


    EU-OPENSCREEN, which integrates high-capacity screening networks throughout Europe, and its partner sites are actively involved in a range of activities to study the new coronavirus SARS-CoV-2, identify therapeutics and search for diagnostics. Efforts include:

    • Exploiting competences in drug discovery with focus on drug repurposing activities and the development of high throughput screening assays for the rapid testing of binders/inhibitors to viral proteins
    • Some partners contribute to the development and implementation of new diagnostic tests for COVID-19
    • Fast access track for scientists wishing to use our pilot compound library for their COVID-19 related research activities
    • Recently submitted H2020 proposal “EUROCOVID”

    Read more here.

    COVID-19 Fast Response Service for medical RIs


    COVID-19 Fast Response Service is a coordinated and accelerated procedure for researchers to access the academic facilities, services and resources of the three medical research infrastructures: the European Research Infrastructure for Translational Medicine (EATRIS), the European Clinical Research Infrastructure network (ECRIN) and the European research infrastructure for biobanking (BBMRI), working together under the umbrella of the Alliance of Medical Research Infrastructures (AMRI). Services include:

    • Biomaterials and associated clinical data (the full list of available resources is available here.)
    • 2019-nCoV challenge studies in NHPs under BSL3+
    • Advanced preclinical models including NHPs, with advanced analytical readouts including molecular and structural imaging (including real time imaging of lung lesions), available under BSL 3 conditions
    • Immunomonitoring and virological assays
    • High throughput screening supporting diagnostics, genotyping, phenotyping and drug repurposing
    • Clinical isolation units
    • Expertise in pharmacology and protein-drug interaction modelling
    • Regulatory support, including:
      • Scientific advice procedure with the European Medicines Agency or national authorities
      • Advice on ethical, regulatory and legal issues in EU member states for clinical trials
      • Ethics approval submissions; initiation and monitoring of recruiting sites
    • Clinical trial support
    • Certified Data centres for the management of clinical trial data

    Read more here.

    Biological and biomedical imaging support for COVID-19 projects


    Biological and biomedical imaging technologies are essential for addressing many research questions – such as those related to the virus, SARS-CoV-2, and the COVID-19 disease it causes – from fundamental research at the molecular and cellular level to medical applications and diagnostics.

    Currently, computed tomography (CT) is the imaging method of choice to diagnose and monitor patients with COVID-19 because of its resolution, availability in intensive care units, and cost-effectiveness. However, most of the available imaging modalities will be centrally involved in research projects aimed at the development of therapeutics and diagnostics to combat coronavirus infection. The need for an in-depth understanding of the molecular processes of the infection will require the design and testing of innovative imaging probes and the access to proper cellular and animal models that are in the domain of Euro-BioImaging Nodes. Moreover the skills in image analysis together with the access to the powerful AI tools will represent an area where our research infrastructure aims to support the biological and biomedical communities.

    Euro-BioImaging continues to support life science research throughout the current pandemic crisis and, where possible, will give priority access to SARS-CoV-2 and COVID-19 related research. Euro-BioImaging’s support includes:

    • Support to users in planning future activities
    • Access to data related to SARS-CoV-2 and COVID-19 research, including via the BioImage Archive
    • Collection of resources useful to SARS-CoV-2 and COVID-19 research

    Read more here.

    Translational medicine: Fast access to key services & facilities 


    EATRIS mission is to accelerate the translation of promising scientific discoveries into benefits for patients. We focus our main activities on bridging the innovation gap between the lab and the clinic and we offer services and expertise to increase chances of research to successfully reach patients.

    The EATRIS infrastructure’s resources are therefore highly relevant for the research community in the context of the COVID-19 pandemic, and include the following expertise and services:

    • 2019-nCoV challenge studies in Non-Human Primates (NHPs) under BSL3+
    • Advanced preclinical models including NHPs, with advanced analytical readouts including molecular and structural imaging (including real-time imaging of lung lesions), available under BSL 3 conditions
    • Immunomonitoring and virological assays
    • High throughput screening supporting diagnostics, genotyping, phenotyping and drug repurposing
    • Clinical isolation units
    • Expertise on pharmacology and protein-drug interaction modelling
    • Regulatory support, including:
      • Scientific advice procedure with the European Medicines Agency or national authorities

    These services are available for any researcher or research team (academic or industrial) that is developing a potential therapy, vaccine or tool for use against the current COVID-19 pandemic, with secured funding. We can also put in touch with the right partners if you are preparing a funding proposal.

    Research requests will be handled via a single point of contact, with a targeted turnaround time of 48 hours or less. This means that applicants will receive details of available services and suppliers within 2 days of the first request. For more information contact Chris Tieken, EATRIS Business Development Manager. Read more here.

    Priority access to structural biology services for COVID-19 research 


    Instruct-ERIC is committed to the use of its infrastructure in response to emerging societal needs. In the case of the COVID-19 virus, Instruct-ERIC would like to ensure that resources are made available to support researchers in their efforts to study the virus, working towards the development of an effective vaccine or treatment.

    Where possible, Instruct-ERIC is offering priority access  for research directly related to COVID-19. Priority access ensures a faster review of research proposals relating to COVID-19. In order to protect staff and users, physical visits to Instruct Centres has been suspended but it may be possible to undertake research remotely during the restricted access period, subject to individual Centre availability.

    In addition, Instruct-ERIC has compiled a list of resources for COVID-19 research, which may be of interest to the wider life science community.

    For enquiries relating to Instruct-ERIC services during the restricted access period, please contact

    Clinical trials


    Clinical research is a critical step for the development and optimisation of solutions for treatment, prevention and diagnostics of COVID. ECRIN provides support to the planning and design of multinational clinical studies, and operational services to the management of the trial. This includes clinical trials on any intervention (medicines, medical devices, procedural intervention), on diagnostics, or on prevention (from behavioural measures through vaccines), and observational studies.

    In the COVID-19 context, ECRIN has established, with its national partners, a COVID-19 taskforce whose mission is to:

    1. Review and digest the scientific literature on COVID clinical trials
    2. Develop a metadata repository for COVID trials making all the non-sensitive COVID-19 trial data accessible
    3. Develop a database on the regulatory, ethical and data protection fast track approvals across all European countries
    4. Ensure preparedness of its national clinical trial unit (CTU) partners for COVID trials
    5. Combine and coordinate national initiatives to promote multinational rather than national trials, including through connection with national funders, sponsors investigators and CTUs
    6. Develop partnership with national and pan-European investigation networks on infectious diseases and intensive care
    7. Outreach to investigators, sponsors, patients, policymakers, funders, and citizens
    8. Initiate international cooperation and outreach, including with WHO and through CRIGH and other initiatives.

    Read more here or contact Sabine Kläger, Head of clinical operations unit

    Computational services for drug development


    As a contribution to the global fight against COVID-19, Instruct-ITALIA has extended its portfolio of services available to users by including a variety of computational services mostly aimed at drug development. The new services include 3D structural modeling, analysis of high-throughput NMR-based screening and modeling of ligand-protein interactions, based also on screening data. Proposals can be submitted via the form at

    Life science data support in COVID-19 research

    ELIXIR Europe

    ELIXIR Nodes provide researchers and consortia working on SARS-CoV-2 with a range of services such as:

    • Data Services and Resources including EMBL-EBI Pathogen Portal, a COVID-19 Beacon and ELIXIR’s recommended interoperability resources.
    • Analysis Tools, Compute Services and other resources. Our infrastructure is contributing to the open global sharing of Galaxy tools and workflows, and offering relevant training courses, a tools registry and access to compute facilities.
    • A record of related ELIXIR publications on SARS-CoV-2.

    For further information on ELIXIR services related to COVID-19, please visit our dedicated page.

    Mouse/rat models for research on vaccines and treatments


    INFRAFRONTIER, the European Research Infrastructure for the generation, phenotyping, archiving and distribution of model mammalian genomes, is fully committed to support researchers around the globe to develop a vaccine against SARS-CoV-2 and to find treatments for COVID-19.

    Resources include:

    • Mouse/Rat models generation, cryopreservation, Phenotyping and Drug validation
    • Fast-track editing of immune-related genes (PMID: 31591574) and genes related to COVID19 research
    • High-dimensional immunophenotyping under normal and under Biosafety Level 3 laboratory (BSL3) conditions relevant to COVID19 research (all lymphoid and myeloid populations found in normal and inflamed tissue parenchyma (lung, intestine…), blood, bronchoalveolar fluid and lymphoid organ
    • Rapid archiving service for the wider scientific community as Covid-19 contingency plans. Sperm freezing.

    And many more. See detailed resource list here.

    High containment facilities for pre-clinical research on SARS-CoV-2/COVID-19


    Research carried out in the ERINHA infrastructure is intended to contribute to the overarching mission of protecting human health by increasing Europe’s preparedness for and capability to respond to an existing high consequence infectious disease or a newly emerged infectious disease threat. Therefore, ERINHA member capacities are highly involved in SARS-CoV-2/COVID-19 research activities.

    Antiviral discovery, drug repurposing and vaccine development are critical to stop pandemics and limit the spread of COVID-19.

    European Research Infrastructure on Highly Pathogenic Agents (ERINHA) provides access to its members – leading European high containment facilities (BSL3 and BSL4) – as well as expertise and project management services to advance research on SARS-CoV-2 / COVID-19.

    Our high containment research capacities include:

    In vitro research capacity:

    • standard virologic assays (e.g. ELISA, PRNT)
    • high throughput SARS-CoV-2 screening assays
    • diagnostic development and testing capacity
    • virus propagation and quantification

    In vivo research capacity:

    • small animal (e.g. mice, rabbits, etc.) disease models
    • Non-Human Primates (NHP) disease models
    • standard in vivo virologic and immunological assays
    • pre-clinical vaccines and therapeutics testing

    Additionally ERINHA provides support for:

    • Coordination of pre-clinical research activities
    • Project management
    • Advice on protocols

    For more information see our COVID-19 research webpage
    To access services, contact ERINHA CCU: contact(at)

    Services for COVID-19 Vaccine Developers


    Researchers developing vaccine candidates against COVID-19 can benefit from TRANSVAC2 services, namely but not exclusively:

    Animal models

    • CEA
    • BPRC
    • IRTA
    • CReSA Centre de Recerca en Sanitat Animal and Helmholtz Centre for Infection Research (HZI)

    Adjuvant formulation

    • HZI

    Clinical Trial Support

    • ECRIN (European Clinical Research Infrastructure Network)

    Regulatory support

    • EATRIS and European Vaccine Initiative

    TRANSVAC is an H2020 project dedicated to accelerate vaccine candidates across the R&D pipeline, by offering services to vaccine developers in academic and industry settings. Visit for more information.

    Additional initiatives from our community

    The following are more initiatives in the fight against COVID-19 within the life science and the research infrastructure communities. To add your initiative, please contact us