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Global collaboration action on climate and health in sub-Saharan Africa is sponsored by European Commission — Horizon Europe. Expected Impact: Expected Impact Projects funded under this topic should contribute towards the reduction of the burden of disease in SSA and thus contribute to achieving SDG 3 ‘Ensure healthy lives and promote well-being for all at all ages and SDG 13, ‘Climate Action’ through increased international cooperation among researchers and funders, catalyse research synergies, and leverage resources and investment. Proposals are expected to include the effective in-kind and/or financial contribution of contributing partners, in order to produce more meaningful and significant effects enhancing the impact of the related research activities. Applicant consortium The contributions from contributing partners should correspond to the amounts they have committed in the letter of endorsement requesting to become a contributing partner (Article 9 Council Regulation (EU) 2021/2085 [1] ). Their contributions can consist of financial contributions and/or in-kind contributions. Applicant contributing partners must submit a first draft of the endorsement letter to the Programme Office before the deadline for submission of the second-stage applications [2] . For details on the process on becoming a Global Health EDCTP3 contributing partner, please consult the Guide for contributing partners . In case of in-kind contribution (even combined with financial contribution), contributing partners become a part of the applicant consortium and participate in the project, as appropriate i.e. as beneficiaries or affiliated entities in the meaning of Article 8 of the Horizon Europe model grant agreement. Also, Global Health EDCTP3 contributing partners can be a country, an international organisation or any public or private legal entity, other than the Global Health EDCTP3 members or their constituent or affiliated entities (please consult the Guide for contributing partners ). Expected Outcome: Background Research shows that 3.6 billion people already live in areas highly susceptible to climate change. Climate change is expected to cause worldwide approximately 250 000 additional deaths per year, from malnutrition, malaria, diarrhea and heat stress between 2030 and 2050 [3] . Despite its low contribution to the drivers of climate change, Africa will bear high consequences of the changing climate, indicated by rising climate-related health emergencies accounting for more than half of public health events recorded in the region over the past two decades [4] : Out of the 2100+ public health events recorded in the African region between 2001 and 2021, 56% were climate-related. The region is witnessing an increase in climate-linked emergencies, with 25% more climate-related events recorded between 2011 and 2021 compared with the previous decade. More particularly, water-borne diseases accounted for 40% of the climate-related health emergencies over the past two decades [5] . Vector-borne diseases, notably yellow fever, accounted for 28% of the climate-related health emergencies, while zoonotic diseases, specifically Congo-Crimean haemorrhagic fever, being the third most prevalent [6] . Where appropriate, a “One Health” approach is recommended to address climate-related public health events. The approach is based on the premise that human, animal and ecosystem health is interconnected and requires a coordinated approach to tackle and resolve the challenges. In addition, vulnerable populations in Africa, particularly the low-income households, women, children, and rural communities, are disproportionately affected by climate change because they face higher exposure to extreme weather, depend heavily on climate-sensitive agriculture productivity, and have limited resources and institutional capacity to adapt, which deepens poverty, food insecurity, health risks, and displacement. Changing climate conditions (such as temperature, humidity and precipitation levels) have an impact on the geographical and seasonal distribution of infectious diseases, with weather affe
Programme areas: Horizon Europe (HORIZON), Global Challenges and European Industrial Competitiveness, Health
Keywords: Animal health, Climate change adaptation, Clinical research, Diagnostics, Drug development, late phases, Early warning systems, Environmental health, Global health, Infectious diseases, Involvement of vulnerable populations, Medical devices, Surveillance, Sustainable development and climate action, Vaccines, Vector control, Africa, Climate, Climate adaptation, Climate sensitive pathogens, Drug development, EDCTP, EDCTP3, Early warning, Enteric diseases, Global Health, Health Interventions, Implementation Research, Infectious Diseases, Late phases, Medical device, Mosquito-borne diseases, Neglected tropical diseases, OneHealth, Prevention, Therapeutics, Vector-borne diseases, Water-borne diseases
Deadline stages: 2026-03-04, 2026-09-17
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EU Funding & Tenders Portal EU Funding & Tenders Portal * Results & Innovation support * SME Self-assessment tool Home Funding Calls for proposals Global collaboration action on climate and health in sub-Saharan Africa Global collaboration action on climate and health in sub-Saharan Africa HORIZON-JU-GH-EDCTP3-2026-02-CH-01-two-stage * Conditions and documents * Partner search announcements HORIZON-JU-GH-EDCTP3-2026-02-two-stage (HORIZON-JU-GH-EDCTP3-2026-02-two-stage) HORIZON-JU-RIA HORIZON JU Research and Innovation Actions HORIZON Action Grant Budget-Based [HORIZON-AG] 04 March 2026 17:00:00 Brussels time 17 September 2026 17:00:00 Brussels time Projects funded under this topic should contribute towards the reduction of the burden of disease in SSA and thus contribute to achieving SDG 3 ‘Ensure healthy lives and promote well-being for all at all ages and SDG 13, ‘Climate Action’ through increased international cooperation among researchers and funders, catalyse research synergies, and leverage resources and investment.
Proposals are expected to include the effective in-kind and/or financial contribution of contributing partners, in order to produce more meaningful and significant effects enhancing the impact of the related research activities.
The contributions from contributing partners should correspond to the amounts they have committed in the letter of endorsement requesting to become a contributing partner (Article 9 Council Regulation (EU) 2021/2085[1]). Their contributions can consist of financial contributions and/or in-kind contributions.
Applicant contributing partners must submit a first draft of the endorsement letter to the Programme Office before the deadline for submission of the second-stage applications[2]. For details on the process on becoming a Global Health EDCTP3 contributing partner, please consult the Guide for contributing partners.
In case of in-kind contribution (even combined with financial contribution), contributing partners become a part of the applicant consortium and participate in the project, as appropriate i.e. as beneficiaries or affiliated entities in the meaning of Article 8 of the Horizon Europe model grant agreement.
Also, Global Health EDCTP3 contributing partners can be a country, an international organisation or any public or private legal entity, other than the Global Health EDCTP3 members or their constituent or affiliated entities (please consult the Guide for contributing partners). Research shows that 3. 6 billion people already live in areas highly susceptible to climate change.
Climate change is expected to cause worldwide approximately 250 000 additional deaths per year, from malnutrition, malaria, diarrhea and heat stress between 2030 and 2050[3].
Despite its low contribution to the drivers of climate change, Africa will bear high consequences of the changing climate, indicated by rising climate-related health emergencies accounting for more than half of public health events recorded in the region over the past two decades[4]: Out of the 2100+ public health events recorded in the African region between 2001 and 2021, 56% were climate-related.
The region is witnessing an increase in climate-linked emergencies, with 25% more climate-related events recorded between 2011 and 2021 compared with the previous decade. More particularly, water-borne diseases accounted for 40% of the climate-related health emergencies over the past two decades [5].
Vector-borne diseases, notably yellow fever, accounted for 28% of the climate-related health emergencies, while zoonotic diseases, specifically Congo-Crimean haemorrhagic fever, being the third most prevalent [6]. Where appropriate, a “One Health” approach is recommended to address climate-related public health events.
The approach is based on the premise that human, animal and ecosystem health is interconnected and requires a coordinated approach to tackle and resolve the challenges.
In addition, vulnerable populations in Africa, particularly the low-income households, women, children, and rural communities, are disproportionately affected by climate change because they face higher exposure to extreme weather, depend heavily on climate-sensitive agriculture productivity, and have limited resources and institutional capacity to adapt, which deepens poverty, food insecurity, health risks, and displacement.
Changing climate conditions (such as temperature, humidity and precipitation levels) have an impact on the geographical and seasonal distribution of infectious diseases, with weather affecting the timing and intensity of disease outbreaks. This results in particular disease-carrying vectors becoming of relevance for Europe.
In addition to climatic factors, regional disease risks are also affected by factors such as land use, vector control, human behaviour, global trade and travel, and public health capacities[7].
Climate change is also increasing Europe’s risk to water-borne diseases by degrading water quality through flooding, heatwaves, and droughts, thereby heightening risks of gastrointestinal infections and other health issues, especially when sanitation and infrastructure are inadequate [8].
With this, the **European Commission’s Strategic Research and Innovation Agenda on Health and Climate Change**[9]– launched in mid‑2025 – sets out a comprehensive R&I roadmap with cross‑cutting priorities including climate‑driven health inequalities, inter‑sectoral data systems, climate adaptation in healthcare systems, and the development of transdisciplinary, global knowledge partnerships (HERA, EC DG RTD, SRIA 2025).
This prioritisation underscores the alignment between the EC’s SRIA and Global Health EDCTP3 objectives, emphasising the need for integrated, equitable, and internationally cooperative research efforts addressing climate-change driven infectious diseases.
Together, these frameworks and epidemiologic trends demonstrate the **urgent need** for Global Health EDCTP3 to fund research on climate-sensitive water- and vector-borne diseases – with a potential dual focus on **sub****‑****Saharan Africa**(SSA), where the burden is high and rising, and **Europe**, where endemic risk is rapidly emerging. In this effort, vulnerable populations in SSA should not be left behind.
Investments in surveillance, climate-adaptive early warning systems, diagnostic and genomic capacity, vector control innovations, One Health approaches, and health system resilience are essential. Aligning with Africa CDC/AU and EC SRIA targets, Global Health EDCTP3 can catalyse cross‑continental innovation, strengthen global health security, and mitigate an escalating threat to relevant vulnerable populations.
Proposals submitted under this topic should aim to deliver results that are contributing to improved health outcomes related to climate sensitive vector- and water-borne pathogens in the scope of the Global Health EDCTP3 SRIA[10] in SSA. In addition, proposals are also expected to lead to: 1.
Improved health outcomes related to climate sensitive vector- and water-borne pathogens in the scope of the Global Health EDCTP3 SRIA with dual focus on SSA and Europe, and/or 2. Enhanced evidence-based decision-making related to mitigating the impact of climate change on the health of SSA populations based on study data, and/or 3.
Increased community and primary health care engagement towards lowering the burden of climate-sensitive vector- and water-borne diseases in the scope of the Global Health EDCTP3 SRIA. Proposals under this topic should include: A/ Minimum one of the following: 1.
Conduct a phase IIb or III clinical trial, or post-authorisation effectiveness (phase IV) trial developing a preventive or therapeutic medicine, or vaccine against the pathogens in scope, OR 2.
Conduct large-scale implementation research on a validated (corresponding to Technology Readiness Level 8) medical device or novel vector control intervention for pathogens in scope in the context of integrated disease control interventions (which may include surveillance systems, early warning tools, diagnostics, and vector control innovations). B/ In addition, proposals should address ALL of the following: 1.
Where appropriate, integrate the OneHealth aspect in the research, the cross-over between human health with environmental and animal health (guidelines EU for OneHealth incorporation in climate and health). Package interventions could also be considered here. 2.
Encompass primary health care systems, community health workers and the community into the study. 3. Include underserved and vulnerable populations such as children under five, pregnant women, elderly people, people with co-morbidities, immunocompromised people, and displaced populations including those living in informal settlements in urban or peri-urban areas as relevant.
C/ In addition, the proposals should address at least two of the following: 1. Include indigenous populations as defined per national/regional context. 2.
Study the impact of climate change on supply chains and access to medical countermeasures. 3. Involve local, regional or national health and climate authorities/policymakers, bridging the gap between research and policymaking.
4. Integrate research in national adaptation plans and National Health Emergency Plans. 5.
Include adaptations of primary health care systems to climate change, for example infrastructural improvements or the training of the primary care workforce. Climate-sensitive infectious diseases are defined in scope of this call as diseases whose incidence, prevalence, or intensity is negatively impacted by climate change and includes the vector- and water-borne pathogens in the scope of the Global Health EDCTP3 SRIA.
Proposals are encouraged to integrate climate-epidemiological models integrating humans, animals and ecosystems under different climate scenarios and to indicate how it will contribute to improving the preparedness of health security related to climate sensitive pathogens in (Southern) EU. Preclinical studies are considered out of scope of the topic.
However, preparatory activities conducted during the preclinical phase can be considered in scope if they enable the conduct of the clinical study/ies in scope (these activities include but are not limited to protocol writing, development/evaluation of laboratory tests, CMC related activities, etc.).
For all Global Collaboration Actions such as this topic, proposals submitted are expected to leverage financial and/or in-kind contributions from contributing partners. Proposals should define the activities of their project in its entirety, including details of the component(s) for which Global Health EDCTP3 funding is requested and the component(s) that are to be financed by contributing partners.
Each contribution should be well described and budgeted in each proposal, so that the activities and related costs that are covered by the in-kind or financial contribution(s) are clearly identified. Applicants are to provide data on the impact of climate change on the chosen disease, and how the proposed study would ameliorate the negative impact.
Applicants will be expected to include a fair representation of health and climate experts and One Health experts in their consortium composition, as relevant, and provide methodologies for translating research findings into public health/climate practice and policy guidelines and are encouraged to follow guidance provided in the EDCTP Knowledge Hub Research into Policy Toolkit.
Multidisciplinary approaches with the integration of adjacent sectors are encouraged (i.e. nutrition, IPC/WASH, etc.). When relevant, proposals should clearly describe the desired target product profile. Applicants need to concisely describe any prior relevant research findings and explain how the proposal builds on available data (including data generated in scope of earlier EDCTP programmes if available).
Full details of the development milestones, including specific go/no-go criteria for the implementation of the proposed clinical trial(s) must be included, as well as specific plans for the subsequent regulatory approval process, which should aim at obtaining relevant market authorisation and an access strategy that will allow patients in low-resource settings to access the final product.
The applicants are encouraged to consider the latest innovations and advances in the clinical trial design and research methods in order to evaluate promising interventions allowing shorter development timings. Applicants are also encouraged to follow the WHO Guidance for best practices for clinical trials.
Proposals should engage communities and relevant stakeholders, most notably (local) key opinion leaders, researchers, health care professionals, policy makers, public health authorities and end-users.
Applicants are reminded of the expectation that proposals should come from research consortia with a strong representation of institutions and researchers from SSA countries, including involvement of Franco/Lusophone countries, if possible. Collaboration with other international research groups with relevant experience is very much encouraged.
Applicants are also reminded of the expectation of reaching out to organisations in countries with relatively lower research capacities. All projects funded under this topic are strongly encouraged to participate in networking and joint activities, as appropriate.
These networking and joint activities could, for example, involve the participation in joint workshops, the exchange of knowledge, and local data collected, the development and adoption of best practices, external conferences joint communication and dissemination activities. Applicants should anticipate budget to cover this collaboration. The details of these joint activities will be defined during the grant agreement preparation phase.
Collaboration and coordination with existing adaptive platform trials in Africa and Europe, EDCTP’s Networks of Excellence and other EDCTP funded initiatives is encouraged, where relevant.
[1] Council Regulation (EU) 2021/2085 of 19 November 2021 establishing the Joint Undertakings under Horizon Europe and repealing Regulations (EC) No 219/2007, (EU) No 557/2014, (EU) No 558/2014, (EU) No 559/2014, (EU) No 560/2014, (EU) No 561/2014 and (EU) No 642/2014 [2] The Global Health EDCTP3 Programme Office will ask the applicant contributing partner to revise the letter in case it significantly departs from the template letter published on the Global Health EDCTP3 website or is missing any compulsory elements.
The final decision as to acceptance or rejection of a new contributing partner rests with the Global Health EDCTP3 Governing Board.
[4] WHO | Africa faces rising climate-linked health emergencies [7] Vector-borne diseases | Health effects | European Climate and Health Observatory Climate-ADAPT [8] Water-borne disease | Health effects | European Climate and Health Observatory Climate-ADAPT [9] Strategic research and innovation agenda on health and climate change - Publications Office of the EU [10] Global Health EDCTP3 Strategic Research and Innovation Agenda The submission session is now available for: HORIZON-JU-GH-EDCTP3-2026-02-CH-01-two-stage Topic conditions and documents #### 1.
Admissibility Conditions: Proposal page limit and layout described in Annex A and Annex E of the Horizon Europe Work Programme General Annexes. **Proposal page limits and layout:** described in Part B of the Application Form available in the Submission System. #### 2.
Eligible Countries described in Annex B of the Work Programme General Annexes. A number of non-EU/non-Associated Countries that are not automatically eligible for funding have made specific provisions for making funding available for their participants in Horizon Europe projects. See the information in the Horizon Europe Programme Guide.
#### 3. Other Eligible Conditions The conditions are described in General Annex B except for the specific conditions for the Global Health EDCTP3 JU funding as regards entities eligible for funding and consortium composition, the specific rule for countries where the coordinator may be established and the obligation to designate a scientific project leader as below.
**Specific conditions replacing the relevant sections in General Annex B to the Horizon Europe Work Programmes** **A. Entities eligible for funding** This section applies to both Research and Innovation Actions (RIA) and Coordination and Support Actions (CSA). To become a beneficiary, legal entities must be eligible for funding.
To be eligible for funding, applicants must be established in one of the following countries: * The Member States of the European Union, including their outermost regions: Austria, Belgium, Bulgaria, Croatia, Cyprus, Czechia, Denmark, Estonia, Finland, France, Germany, Greece, Hungary, Ireland, Italy, Latvia, Lithuania, Luxembourg, Malta, Netherlands, Poland, Portugal, Romania, Slovakia, Slovenia, Spain, Sweden; * The Overseas Countries and Territories (OCTs) linked to the Member States: Aruba (NL), Bonaire (NL), Curação (NL), French Polynesia (FR), French Southern and Antarctic Territories (FR), Greenland (DK), New Caledonia (FR), Saba (NL), Saint Barthélemy (FR), Sint Eustatius (NL), Sint Maarten (NL), St.
Pierre and Miquelon (FR), Wallis and Futuna Islands (FR); * Countries associated to Horizon Europe[The list is correct at the time of adoption of this work programme. Please see the Horizon Europe List of Participating Countries on the Funding & Tenders Portal for up-to-date information on the current list and on the position for Associated Countries: [https://ec. europa.
eu/info/funding-tenders/opportunities/docs/2021-2027/common/guidance/list-3rd-country-participation_horizon-euratom_en.
pdf]]: Albania, Armenia, Bosnia and Herzegovina, Canada (associated to Pillar II 'Global Challenges and European Industrial Competitiveness', including for the institutionalised European partnerships, and for award procedures implementing Union budget for the year 2024 and onwards), Faroe Islands, Georgia, Iceland, Israel, Kosovo[[This designation is without prejudice to positions on status and is in line with UNSCR 1244/1999 and the ICJ Opinion on the Kosovo declaration of independence.]]
, Moldova, Montenegro, New Zealand (associated to Pillar II 'Global Challenges and European Industrial Competitiveness' as from the Work Programmes 2023 onwards, including for the institutionalised European partnerships), North Macedonia, Norway, Serbia, Republic of Korea (Pillar II only), Switzerland, Tunisia, Turkey, Ukraine, United Kingdom; * Until association agreements start producing legal effects either through provisional application or their entry into force, transitional arrangements apply.
The transitional arrangements apply, at the time of the adoption of this Work Programme, with regard to the following countries and legal entities established in these countries, with which association negotiations are being processed or where association is imminent): Egypt, Morocco, . * The following countries which are constituent states of the EDCTP Association[The list is correct at the time of adoption of this work programme.
For an update, please check the EDCTP Association website [www. edctp. org.]]
: Benin, Burkina Faso, Burundi, Cameroon, Côte d’Ivoire, Democratic Republic of the Congo, Ethiopia, Eswatini, Gabon, The Gambia, Ghana, Guinea-Bissau, Guinea-Conakry, Kenya, Liberia, Malawi, Mali, Mozambique, Namibia, Niger, Nigeria, Republic of the Congo, Rwanda, Senegal, Sierra Leone, Somalia, South Africa, Tanzania, Uganda, Zambia, Zimbabwe.
Legal entities which are established in countries not listed above (including in low-and middle-income countries that are not members of the EDCTP Association) will be eligible for funding if provided for in the specific call topic conditions, or if their participation is considered essential for implementing the action by the granting authority. **B.
Consortium composition** Unless otherwise provided for in the specific call conditions, for all actions, due to the policy objectives of Global Health EDCTP3, legal entities forming a consortium are eligible to participate in actions under the programme provided that the consortium includes as beneficiaries: * At least three legal entities independent from each other and each established in a different country, where legal entities are eligible to receive funding; * At least one independent legal entity established in a Member State, or in an associated country to Horizon Europe that is a member of the EDCTP Association; and * At least one independent legal entity established in a sub-Saharan African country that is a member of the EDCTP Association.
This condition applies to both Research and Innovation Actions (RIA) and Coordination and Support Actions (CSA). For the two CSA (2) topics under call HORIZON-JU-GH-EDCTP3-2026-03 in case the applicant consortia opt for including the EDCTP Association as coordinator, the EDCTP Association must not be counted as one of the three independent legal entities necessary to ensure the eligibility of the consortium composition.
**Affiliated entities**— Affiliated entities are eligible for funding under the same conditions as beneficiaries.
**Associated partners**— Entities not eligible for funding and therefore not able to participate as beneficiaries or affiliated entities (i.e. entities which participate in the action without signing the grant agreement, and without the right to charge costs or claim contributions) are allowed, subject to any conditions regarding associated partners set out in the specific call conditions.
**International organisations** – International European research organisations are eligible to receive funding. Other international organisations are not eligible to receive funding unless their participation is considered essential for implementing the action by the granting authority.
International organisations with headquarters in a Member State or associated country are eligible to receive funding when provided for in the specific call conditions.
**Specific rules regarding legal entities that may be the coordinator of an indirect action** In accordance with Article 110(2) of the Council Regulation 2021/2085 establishing the Joint Undertakings under Horizon Europe[[Council Regulation (EU) 2021/2085 of 19 November 2021 establishing the Joint Undertakings under Horizon Europe and repealing Regulations (EC) No 219/2007, (EU) No 557/2014, (EU) No 558/2014, (EU) No 559/2014, (EU) No 560/2014, (EU) No 561/2014 and (EU) No 642/2014_, p.
17–119_.]] , where entities established in a third country without an agreement to protect the financial interests of the Union participate with funding in an indirect action, the coordinator of the indirect action must be established in a Member State or associated country, or South Africa.
**Scientific project leader** If the coordinator is not established in a country in SSA (_please see previous paragraph_), the designation of a scientific project leader established in a SSA country member of the EDCTP Association with the roles as described below is mandatory. A work package on ‘scientific project leadership’ must be included in the proposals and budget needs to be provided for this activity.
The scientific project leader oversees the project scientific governance and leadership. For this purpose, proposals must include a work package where the details of scientific project leadership are laid down. The scientific project leader should indicatively perform the following tasks: * During the call for proposals and selection process, coordinate meetings on and drafting of the full project proposal.
* Work with the coordinator and other beneficiaries on the drafting and negotiation of the consortium agreement and other legal agreements among the beneficiaries.
* Act as the key contact point for the Global Health EDCTP3 JU regarding all scientific action governance issues, steer and provide oversight in the development of the scientific actions, without prejudice to the tasks entrusted directly to the coordinator as per the Model Grant Agreement.
* Support and collaborate with the coordinator on its monitoring activities and the adoption of appropriate internal measures, to ensure that beneficiaries are fulfilling their obligations regarding budget, timeline, deliverables, and scientific quality. * Review the action’s deliverables and reports before their submission by the coordinator. * Lead the work packages(s) related to the tasks of scientific project leadership.
Annex 1 to the grant agreement and the consortium agreement should address the relationship of the scientific project leader with the coordinator regarding their respective tasks, for example sharing of the information received from or sent to Global Health EDCTP3 on all issues of interest for the proper scientific management of the action. described in Annex B of the Work Programme General Annexes. #### 4.
Financial and operational capacity and exclusion described in Annex C of the Work Programme General Annexes. #### 5a. Evaluation and award: Award criteria, scoring and thresholds are described in Annex D of the Work Programme General Annexes.
#### 5b. Evaluation and award: Submission and evaluation processes **Specific conditions related to Scores and weighting** **Replacing the scores and weighting section in General Annex D to the Horizon Europe Work Programmes as regards second stage of two-stage evaluations, for Research and Innovation Actions (RIA). **Evaluation scores will be awarded for the criteria, and not for the different aspects listed in the table.
For full applications, each criterion will be scored out of 5. The threshold for individual criteria 1 (Excellence) and 2 (Impact) will be 4 and for criterion 3 (Quality and Efficiency of the implementation) will be 3. The overall threshold, applying to the sum of the three individual scores, will be 12.
Proposals that pass the individual threshold and the overall threshold will be considered for funding, within the limits of the available call budget. Other proposals will be rejected. _Nota bene: for the CSAs and the first stage of the two-stage evaluation of RIAs, the scores and weighting as indicated in Annex D of the General Annexes of the Horizon Europe work programme 2023/2025 apply.
_ In addition to the aspects of award criteria included in General Annex D, the following aspects are taken into consideration during the evaluation of second-stage proposals: For the ‘impact’ criterion: Production of meaningful and significant effects enhancing the impact of the relevant research activities via the inclusion of effective in-kind and/or financial contribution of contributing partners.
For the ‘quality and efficiency of the implementation’ criterion: Leveraging of financial and/or in-kind contributions from contributing partners that are equal or greater than the requested JU contribution, in order to ensure the necessary resources and effort for the action. #### 5c. Evaluation and award: Indicative timeline for evaluation and grant agreement described in Annex F of the Work Programme General Annexes.
#### 6. Legal and financial set-up of the grants Implementing the provision on affordable access as defined in Article 114 of the Council Regulation 2021/2085[[Council Regulation (EU) 2021/2085 of 19 November 2021 establishing the Joint Undertakings under Horizon Europe and repealing Regulations (EC) No 219/2007, (EU) No 557/2014, (EU) No 558/2014, (EU) No 559/2014, (EU) No 560/2014, (EU) No 561/2014 and (EU) No 642/2014, _p. 17_.]]
, grants awarded under this topic will have to include in their Plan for the exploitation and dissemination of results including communication activities to be submitted during the project as a deliverable also the following: Participants must include in their Plan for the exploitation and dissemination of results[[For more information on the Plan for the exploitation and dissemination of results, please consult the General Annexes of Horizon Europe Work Programmes.]]
an appropriate and proportionate access plan that demonstrates their strategies to ensure that the products and services that they develop based or partly based on the results of clinical studies undertaken by their project are affordable, available and accessible to the public (market and end-users) at fair and reasonable conditions.
This covers registration targets, plans to meet demand, flexible approaches to IP, engagement with regulators and manufacturers where relevant and other strategies that reflect ability to pay and ensures that economic barriers to access are low.
In addition, participants should add, if relevant, as part of the plan, an outline on how to achieve the optimal use of an intervention including, for example, how to avoid irrational use, overuse or abuse (e.g. antimicrobials). The plan is to be submitted with the second-stage proposal.
In addition to any updates during the project, a final version of the Plan for the exploitation and dissemination of results including the above access plan, must also be submitted with the final report of the project.
Also in line with Article 114 of the Council Regulation 2021/2085[[Council Regulation (EU) 2021/2085 of 19 November 2021 establishing the Joint Undertakings under Horizon Europe and repealing Regulations (EC) No 219/2007, (EU) No 557/2014, (EU) No 558/2014, (EU) No 559/2014, (EU) No 560/2014, (EU) No 561/2014 and (EU) No 642/2014]], participants will be subject to the following additional exploitation obligations: 1.
Participants must – up to four years after the end of the action (see Data Sheet, Point 1) – use their best efforts to ensure that resulting health technologies and services will be broadly available and accessible, as soon as possible and at fair and reasonable conditions.
In this respect, if, despite a participants’ best efforts, the results are not exploited within one year after the end of the action, participants must (unless otherwise agreed in writing with the granting authority) use the Horizon Results Platform to find interested parties to exploit the results. 2.
In case the participants cannot fulfil the preceding obligation, the participants must (if requested by the granting authority) grant non-exclusive licences - under fair and reasonable conditions - to their results to legal entities that commit to rapidly and broadly exploiting the resulting health technologies and services and ensure that they are broadly available and accessible, as soon as possible and at fair and reasonable conditions.
3. In case of transfer of the ownership or licensing of results, participants must pass on such additional exploitation obligations to the legal entities exploiting the results. 4.
For up to four years after the action (see Data Sheet, Point 1), the funding body must be informed every year about the status of the development of the product and any other exploitation of the results through an annual report that is due on each anniversary of the end of the grant agreement. described in Annex G of the Work Programme General Annexes.
**JU right to object to transfer/exclusive licensing** Global Health EDCTP3 may, up to four (4) years after the end of the action, object to a transfer of ownership or to the exclusive licensing of results, as set out in the specific provision of Annex 5 of the Model Grant Agreement.
In addition, in accordance with Article 24(3) of Council Regulation 2021/2085 establishing the Joint Undertakings under Horizon Europe[[Council Regulation (EU) 2021/2085 of 19 November 2021 establishing the Joint Undertakings under Horizon Europe and repealing Regulations (EC) No 219/2007, (EU) No 557/2014, (EU) No 558/2014, (EU) No 559/2014, (EU) No 560/2014, (EU) No 561/2014 and (EU) No 642/2014, _p. 17_.]]
and the Model Grant Agreement, the right to object applies also to participants that have not received funding from the JU. [1] Council Regulation (EU) 2021/2085 of 19 November 2021 establishing the Joint Undertakings under Horizon Europe and repealing Regulations (EC) No 219/2007, (EU) No 557/2014, (EU) No 558/2014, (EU) No 559/2014, (EU) No 560/2014, (EU) No 561/2014 and (EU) No 642/2014, p. 17.
**Information sharing regarding the proposals and the evaluation results** Applicants should be aware that the following information regarding their proposals may be shared with the members of the JU Committee of the EDCTP Association: 1. Following eligibility check of the applications: aggregated country level data i.e. number of applicants, funding requested, organisation type; 2.
For successful proposals, following Global Health EDCTP3 Governing Board decision on the call evaluation results: number; acronym; title; duration; role; country; legal name; PIC; legal type; total cost; requested JU contribution; 3.
Regarding project information following Grant Agreement (GA) signature: signature date of the GA; number, acronym, title, and duration of projects; role, country, legal name, PIC, legal type, URL, total cost, requested JU contribution, FC received, FC given, and IKOP of participants; 4.
Under specific conditions and following Global Health EDCTP3 Governing Board approval of the request of EDCTP Association, for proposals on the reserve list and unsuccessful proposals: number; acronym; title; duration; role; country; legal name; PIC; legal type; total cost; requested JU contribution.
**Access to information and involvement of contributing partners** To promote transparency and accountability, Global Health EDCTP3 may invite any contributing partners providing financial contributions under a certain topic to propose one representative as observer to participate in the evaluation process under confidentiality safeguards.
This possibility does not apply to contributing partners that are part of a consortium submitting a proposal under the relevant topic.
**Documents and information** By applying under any topic, participants consent that the JU reserves the right to share information and documents relevant to their application and where applicable their grant agreement and its implementation with contributing partners as identified and providing financial contributions under the relevant topic.
This information and documentation will only be shared under confidentiality safeguards for policy and monitoring purposes. They include: Global Health EDCTP3 may consult the relevant contributing partners for the purpose of assessing the project reports and deliverables.
For all projects under this topic, if the coordinator is not from a country in SSA, the designation of a scientific project leader with the roles as described in the introduction is mandatory. A work package on ‘scientific project leadership’ must be included in the proposals and budget needs
According to the current listing, eligibility includes: Open to legal entities established in EU Member States and countries associated to Horizon Europe (including EEA/EFTA countries, and other associated third countries). Action type: HORIZON-JU-RIA HORIZON JU Research and Innovation Actions. Additional conditions: "> General conditions 1. Admissibility Conditions: Proposal page limit and layout described in Annex A and Annex E of the Horizon Europe Work Programme General Annexes. Proposal page limits and layout: described in Part B of the Application Form available in the Submission System. 2. Eligible Countries described in Annex B of the Work Programme General Annexes. A number of non-EU/non-Associated Countries that are not automatically eligible for funding have made specific provisions for making... See the official call documentation on the F&T Portal for full eligibility criteria and participation rules. Confirm the full requirements in the official notice before applying.
The published deadline was March 4, 2026, which has passed. Check the official notice for any future application windows before investing time in a proposal.
Global collaboration action on climate and health in sub-Saharan Africa is funded by European Commission — Horizon Europe. Verify program details on the funder's official page before applying.
Start from the official opportunity page linked in this listing — it carries the sponsor's submission instructions.
Reinforcing EU autonomous access to space through EU-based spaceports is sponsored by European Commission — Horizon Europe. Expected Outcome: Project results are expected to contribute to all of the following outcomes: Reinforcing EU strategic autonomy by reducing non-EU dependencies for accessing space; Providing an EU access to space necessary for EU space missions through state of the art and innovative solutions; Diversifying the access to space providers in the EU; Contributing to expand commercial access to space offers and services in the EU; Reinforcing Access to Space to ensure that Europe maintains and improve autonomous, reliable and cost-effective access to space. Scope: The EU needs to improve the resilience of its access to space for the implementation of EU space programme. New entrants will contribute to this endeavour. Projects are expected to support EU launch service providers to set up launch pad(s) in the EU territory enabling to perform EU launch services. Projects are expected to contribute to the development of necessary ground facilities to conduct launch services from the EU territory; e.g. launch integration, storage and operation facilities, launch pad and complex, control command facility, payload processing and integration facilities, tracking means, safety means, propellant storage... EU launch service provider(s) are expected to be part of the project consortium and be the ultimate users of the resulting facilities making use of EU launch vehicles for providing EU launch services. Proposals under this topic should explore synergies and be complementary to past actions related to ground segment for launch services, in particular the topics: HORIZON-CL4-2023-SPACE-01-23 and HORIZON-CL4-2025-02-SPACE-11. All the activities should be complementary with national and ESA on-going or future activities, in particular those decided at the ESA council Ministerial Meeting in November 2025. In this topic, the integration of the gender dimension (sex and gender analysis) in research and innovation content should be addressed only if relevant in relation to the objectives of the research effort. Technology Readiness Level - Technology readiness level expected from completed projects Activities are expected to achieve TRL 8 by the end of the project. The reference TRL definition is the ISO 16290:2013 applicable to the space sector. Programme areas: Horizon Europe (HORIZON), Global Challenges and European Industrial Competitiveness, Digital, Industry and Space
Space critical Equipment for EU non-dependence – Space Refuelling Interface is sponsored by European Commission — Horizon Europe. Expected Outcome: Project results are expected to contribute to all of the following expected outcomes: Reinforcing EU strategic autonomy by reducing non-EU dependencies on critical space Equipment and related technologies across their entire supply chain; Providing unrestricted access to critical space Equipment and related technologies relevant for EU space missions and pilots (e.g. In-Orbit Space Operations); Developing or regaining capacity to operate independently in space by developing resilient space Equipment and related technologies supply chains, relying on EU supply chains and/or trustable and reliable supply chains not affected by non-EU export restrictions; Enhancing competitiveness by developing products and capabilities reaching equivalent or superior performance level than those from outside the EU and compete at worldwide level. Scope: Unrestricted access to state-of-art space equipment and related technologies is a pre-requisite for the EU space industry responding to EU space missions. However, especially for some families of equipment, the available solutions in EU do not meet the current high-performance space requirements. Currently, alternative products sourced from outside EU, are either affected by non-EU export control, that limits its use, or present challenges in terms of trustable supply chains for the implementation of EU space missions with a security dimension. Within the frame of this topic, it is expected to finance and implement a development project aiming at maturing critical equipment with the final goal of lowering the dependency from outside EU. This will be done by establishing a long-term sustainable supply chain for supporting EU strategic autonomy in the space sector. The selection of the supply chains shall reflect this objective. Therefore, the supply chain shall preferably be built fully based in EU and when this can only be achieved partially, services procured from outside EU shall nevertheless ensure that the overall supply chain will remain trustable and not affected by non-EU export control. The latest scenario is subject to the approval of the granting authority (i.e. DG-DEFIS and HaDEA). The space equipment and related technologies relevant for this topic represent a direct implementation of the EU Observatory of Critical Technologies (OCT) Technology Roadmap, named Robotics Manipulators for Space Applications: Space Refuelling Interface . Further details will be provided at the latest at the opening of the Call, in a Guidance document published on the Funding & Tenders Portal. Space is a low volume market affected by a dynamic industrial landscape compared to the terrestrial market therefore, technological spin in and/or bilateral collaborations should be enhanced between European non-space and space industries. Furthermore, proposed activities should be complementary to relevant national or other activities at EU level. Complementary activities should be clearly identified, described and the proposal should report how the complementarity is ensured. To achieve the non-dependence objective, applicants are expected to include a dedicated proposal’s paragraph covering: The description of the technology and/or technology processes used for developing the equipment and high-level breakdown of the supply chain to be used. Applicants should demonstrate that the supply chain and final product are free of any legal export restrictions or limitations, such as those established in the International Traffic in Arms Regulations (ITAR) or equivalent instruments applicable in other non-EU jurisdictions. Applicants shall also report, in a dedicated subsection, if and which part of the supply chain is affected by non-EU export controls such as the Export Administration regulation (EAR) i.e. EAR99. The description of the suitable technology development process that has been identified and set up within the consortium for avoiding export restrictions of non-EU states and assess vulnerab Programme areas: Horizon Europe (HORIZON), Global Challenges and European Industrial Competitiveness, Digital, Industry and Space, Space, including Earth Observation
IA Resilience call reinforcing Europe's strenght in health is sponsored by European Commission — Horizon Europe. Expected Outcome: the proposals under this call are expected to address one or more of the following subjects : • Enhanced personalized monitoring, care and treatments, focusing on the development of highly customized healthcare solutions, including the required research and diagnostic tools, tailored to individual needs, covering various scenarios such as chronic disease management, physiotherapy, precision diagnosis, personalized medicine/treatment, pre- and postoperative care, and daily assistance in homes and common spaces. It also targets effective management of chronic diseases and elderly care through personalized monitoring and interventions facilitated by advanced sensor technologies and edge-to-cloud solutions. This includes the development and integration of solutions for Hospitalization at Home, enabling patients to receive complex, remotely supervised care using intelligent medical devices capable of sensing, analysing, and transmitting real-time data. This requires a continuum, from in-hospital diagnostics to robust, long-term patient support at home via AI-driven care pathways and hospitalization at home. • Prevention and treatment of diseases, allowing the improved scientific understanding, early detection and proactive prevention of diseases through scientific research, continuous monitoring, predictive analytics, and timely alerts, possibly powered by AI algorithms. This preventive approach enables early intervention and significantly reduces risks associated with many illnesses such as viral infections (e.g. epi- and pan demics), cardiovascular diseases, diabetes complications affecting the health of the young and old. • Efficient, scalable, and cost-effective healthcare, demonstrating how ECS-based technologies can streamline clinical workflows, reduce administrative burdens, and improve resource allocation in healthcare systems. This includes automation and intelligent operations management across clinical, diagnostic, and homecare settings, ultimately improving cost-effectiveness and scalability. • Secure and compliant healthcare continuum, including solutions that ensure robust data protection and regulatory compliance (e.g. GDPR), particularly in handling sensitive health data. Projects should adopt privacy-by-design principles and implement secure data handling architectures using localized edge computing, encryption, authentication, and anonymization strategies within both clinical and assisted living environments. • Seamless interoperability across devices, systems, and platforms, addressing the integration of heterogeneous systems across the edge-to-cloud continuum. Solutions should rely on open standards and modular architectures to ensure interoperability, flexibility, and adaptability across various healthcare settings and use cases, fostering a unified European health-tech ecosystem. Programme areas: Horizon Europe (HORIZON), Global Challenges and European Industrial Competitiveness, Digital, Industry and Space
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