Month: September 2021

European Partnership for Fostering a European Research Area for Health (ERA4Health)

The European Partnership for Fostering a European Research Area for Health (ERA4Health) is a partnership bringing together 37 entities from 24 countries. It aims to support transnational medical research in prevention, diagnosis, treatment, capacity building, and responsible research and innovation (RRI).
In 2024, three calls for proposals were published:
• NutriBrain, focusing on modulation of brain ageing through nutrition and healthy lifestyle (closed)
• NANOTECMEC, focusing on nano and advanced technologies for disease prevention, diagnosis, and therapy (closed)
• EffecTrial, focusing on pragmatic comparative effectiveness studies in non-communicable diseases (open)

EU Mission on Cancer

One of five EU Missions, the Mission on Cancer, together with Europe’s Beating Cancer Plan, aims to provide a better understanding of cancer, allow for earlier diagnosis and optimisation of treatment and improve cancer patients’ quality of life during and beyond their cancer treatment. The Mission aims to support: an understanding of cancer, prevention and early detection, diagnosis and treatment, and quality of life for patients and their families.
In 2024, a call for proposals was published, covering six topics under Research and Innovation Actions (RIA) (closed).

European Research Centre (ERC) Synergy Grant

The European Research Council (ERC) supports frontier research in any field. It is open to investigators worldwide, as long as the host institution (HI) of the principal investigator that receives ERC funding is established in a Member State or a country associated to Horizon Europe. The ERC has four major grant programmes: Starting Grants, Consolidator Grants, Advanced Grants, and Synergy Grants.
The ERC Synergy Grant supports joint projects of multiple researchers focusing on research problems that could not be solely addressed by one principal investigator.
Under the 2024 work programme, one call for proposals was published (closed).

European Research Council (ERC) Proof of Concept

The European Research Council (ERC) supports frontier research in any field. It is open to investigators worldwide, as long as the host institution (HI) of the Principal Investigator (PI) that receives ERC funding is established in a Member State or a country associated to Horizon Europe.
The ERC Proof of Concept programme supports the further development of projects funded by other ERC support programmes in an earlier stage.
A call for proposals was published in November 2024, with multiple cut-off dates in 2025.

European Research Centre (ERC) Advanced Grants

The European Research Council (ERC) supports frontier research in any field. It is open to investigators worldwide, as long as the host institution (HI) of the principal investigator that receives ERC funding is established in a Member State or a Country Associated to Horizon Europe. The ERC has four major grant programmes: Starting Grants, Consolidator Grants, Advanced Grants, and Synergy Grants.
The ERC Advanced Grant supports leading researchers with noteworthy accomplishments who wish to obtain long-term funding for ambitious research projects. The European Research Centre Advanced Grants are dedicated to experienced scientists who want to pursue groundbreaking and high-risk projects.
In 2024, a call for proposals was published (closed). In 2025, a call for proposals is expected to open in May.

European Research Council (ERC) Consolidator Grant

The European Research Council (ERC) supports frontier research in any field. It is open to Principal Investigators (PIs) worldwide, as long as the Host Institution (HI) of the principal investigator that receives ERC funding is established in a Member State or a country associated to Horizon Europe. The ERC has four major grant programmes: Starting Grants, Consolidator Grants, Advanced Grants, and Synergy Grants.
The ERC Consolidator Grant supports researchers with 7-12 years of experience.
A call for proposals opened in September 2024 and will close in January 2025.

European Research Council (ERC) Starting Grant

The European Research Council (ERC) supports frontier research in any field. It is open to investigators worldwide, as long as the host institution (HI) of the principal investigator that receives ERC funding is established in a Member State or a country associated to Horizon Europe. The ERC has four major grant programmes: Starting Grants, Consolidator Grants, Advanced Grants, and Synergy Grants. The ERC Starting Grant programme supports early-career scientists developing a wide range of innovative projects.
In 2024, a call for proposals was published (closed).

European Partnership for Pandemic Preparedness

The European Partnership on Pandemic Preparedness aims to improve the European Union’s (EU) preparedness to predict, prevent and respond to emerging infectious health threats by better coordinating funding for research and innovation at EU, national (and regional) levels.
In 2024, a calls for proposals was published to launch the partnership (closed).

European Partnership on One-Health Anti-Microbial Resistance (OH AMR)

The One Health Antimicrobial Resistance (OH AMR) partnership aims to support the coordination and alignment of AMR research activities and funding in Europe and beyond. The main goal is to contribute to achieving the objectives of the European One Health Action Plan against AMR and the World Health Organization (WHO) Global Action Plan on AMR by reducing the threat of AMR and contributing to achieving the objectives of the Health Emergency Preparedness and Response Authority (HERA).
In 2024, one call for proposals was published under the topic Tackling diseases and reducing disease burden (closed).

European Partnership for Personalised Medicine (EP PerMed)

The European Partnership for Personalised Medicine (EP PerMed) supports synergies in research on personalised medicine across the European Union (EU) and its regional partners. The main objectives of the partnership are to (i) ensure a faster uptake of research and innovation (R&I) results into clinical practice and secure Europe’s position in state-of-the-art healthcare provision; (ii) facilitate approaches that take into account individual differences and better utilise the accumulating data to manage health, disease and its predisposition; (iii) contribute towards more sustainable healthcare systems and independence in data intensive healthcare.
In 2024, one call for proposals was published (closed). A new call for proposals is expected to be opened in mid-December 2024: Joint Transnational Call (JTC) 2025, which aims to fund human health research on pharmacogenomic strategies for personalised medicine approaches. The call will close in June 2025, and the project is expected to start at the end of 2025/beginning 2026.

What type of funding are you looking for?

  • Grant:
    Grants are direct financial contributions from the European Union budget awarded by way of a donation to third-party beneficiaries (usually non-profit-making organisations) engaged in activities that serve EU policies.
  • Loan:
    Loans are measures of financial support provided on a complementary basis from the budget in order to address specific policy objectives of the European Union. Such instruments are implemented in partnership with public and private institutions such as banks, venture capitalists or angel investors.

What stage of development are you seeking R&I funding for?

  • Basic science: Basic science covers the various exploratory steps even prior to discovery
  • Discovery: Drug discovery aims to find potential disease-altering targets, such as a gene or a protein in humans. Prior to testing candidate compounds for safety
  • Preclinical development: Preclinical development concerns the testing of candidate compounds for safety in specific indications or disease conditions. Introduction of candidate compound in living biological systems (animals)
  • Phase 1 clinical trials: These are the first clinical trials on humans(usually 20-80 volunteers) testing the safety, side effects, best dose, and timing of a new treatment
  • Phase 21/2b clinical trials: This is the follow-up trial with roughly 100 to 500 patients to analyse efficacy and safety
  • Phase 3 clinical trials: These trials usually involve several hundreds to many thousands patients and tests the results of earlier clinical trials on larger populations to generate robust data on safety, efficacy and benefit-risk relationships of the medicine. Comparison to placebo and/or active comparator (best standard treatment)
  • Registration & launch: This concerns post-study, prior to launch, activities related to market launch. That can include, among others, marketing authorisation, regulatory activities, post-study communication or HTA
  • Introduction & delivery: This concerns all post-launch activities

What do you want to develop?

  • Treatment or vaccine:
    Refers to a drug or vaccine
  • Diagnostic or medical device:
    Refers to diagnostics and medical devices
  • Platform:
    Refers to a digital health platform or medical app
  • Knowledge:
    Refers to conducting research to help build our understanding on a topic
  • Standards:
    Refers to creating a benchmark for a specific issue

What type of organisation are you?

  • Small & medium-sized enterprises:
    <250 employees, annual revenue <EUR 50,000,000) or balance sheet < EUR43 million. This applies to individual firms only. If part of larger group, check the User Guide: https://ec.europa.eu/docsroom/documents/42921
  • Large enterprises:
    >250 employees or annual revenue > EUR 50,000,000. Non-profit organisation (non-governmental organisations that are recognised with a non-profit status)
  • Non-profit organisations:
    Non-governmental organisations that are recognised with a non-profit status
  • Academic:
    Linked to a university or equivalent
  • Public:
    Local, regional, federal government representative

What stage of diagnostics development does your research aim to cover?

  • Development:
    Product development
  • Validation:
    Lab and clinical validation
  • Evaluation & Authorisation:
    Regulatory approvals
  • Access:
    Monitoring

What stage of medicine or vaccine development does your research aim to cover?

  • Discovery and development:
    Identification of promising compounds for development and initial experiments to gather information
  • Preclinical research:
    Laboratory and animal testing to answer basic questions about safety
  • Phase 0 (clinical):
    Testing on limited number of subjects at subtherapeutic doses
  • Phase I (clinical):
    Testing on <100 healthy subjects with the disease/condition
  • Phase II (clinical):
    Testing on up to several hundred subjects with the disease/condition
  • Phase III (clinical):
    Testing on 300 to 3,000 volunteers with the disease/condition
  • Preregistration / Phase IV (clinical):
    Testing on several thousand volunteers with the disease/condition
  • Clinical (unspecified):
    Clinical phase unknown
  • Evaluation & Authorisation:
    Activities relating to marketing authorisation
  • Access:
    Monitoring

Where are you based?

  • Africa : Algeria, Angola, Benin, Botswana, Burkina Faso, Burundi, Cabo Verde, Cameroon, Central African Republic (CAR), Chad, Comoros, Congo (Democratic Republic of the), Congo (Republic of the), Cote d’Ivoire, Djibouti, Egypt, Equatorial Guinea, Eritrea, Eswatini, Ethiopia, Gabon, Gambia, Ghana, Guinea, Guinea-Bissau, Kenya, Lesotho, Liberia, Libya, Madagascar, Malawi, Mali, Mauritania, Mauritius, Morocco, Mozambique, Namibia, Niger, Nigeria, Rwanda, Sao Tome and Principe, Senegal, Seychelles, Sierra Leone, Somalia, South Africa, South Sudan, Sudan, Tanzania, Togo, Tunisia, Uganda, Zambia, Zimbabwe
  • America (non-US & Canada) : Antigua and Barbuda, Argentina, Bahamas, Barbados, Belize, Bolivia, Brazil, Chile, Colombia, Costa Rica, Cuba, Dominica, Dominican Republic, Ecuador, El Salvador, Grenada, Guatemala, Guyana, Haiti, Honduras, Jamaica, Mexico, Nicaragua, Panama, Paraguay, Peru, Saint Kitts and Nevis, Saint Lucia, Saint Vincent and the Grenadines, Suriname, Trinidad and Tobago, Uruguay, Venezuela
  • Asia-Pacific : Afghanistan, Australia, Bangladesh, Bhutan, Burma, Brunei, Cambodia, China (including special administrative regions of Hong Kong and Macau), Cook Islands, Federated States of Micronesia, Fiji, India, Indonesia, Japan, Kiribati, Laos, Malaysia, Maldives, Marshall Islands, Mongolia, Nepal, New Caledonia, New Zealand, Niue, North Korea, Pakistan, Palau, Papua New Guinea, Philippines, Singapore, Solomon Islands, South Korea, Sri Lanka, Taiwan, Thailand, Timor-Leste, Tonga, Tuvalu, Vanuatu, Vietnam
  • Europe (non-EU) : Albania, Andorra, Armenia, Azerbaijan, Belarus, Bosnia and Herzegovina, Georgia, Iceland, Kosovo, Liechtenstein, Moldova, Monaco, Montenegro, North Macedonia, Norway, Russia, San Marino, Serbia, Switzerland, Turkey, Ukraine, United Kingdom
  • European Union (EU) : Austria, Belgium, Bulgaria, Croatia, Republic of Cyprus, Czech Republic, Denmark, Estonia, Finland, France, Germany, Greece, Hungary, Ireland, Italy, Latvia, Lithuania, Luxembourg, Malta, Netherlands, Poland, Portugal, Romania, Slovakia, Slovenia, Spain, Sweden
  • Middle East : Cyprus, Lebanon, Syria, Iraq, Iran, Israel, Jordan, Saudi Arabia, Kuwait, Qatar, Bahrain, United Arab Emirates, Oman, Yemen
  • United States (US) & Canada : United States, Canada

What type of organisation are you?

  • Small and medium-sized enterprise (SME):
    Staff headcount 50 < and turnover ≤ EUR 10 m or balance sheet total ≤ EUR 10 m (small); Staff headcount 250 < and turnover ≤ EUR 50 m or balance sheet total ≤ EUR 43 m (medium)
  • Large enterprise:
    Staff headcount > 250
  • Non-profit organisation:
    Association, foundation, or equivalent
  • Academic:
    University, research institute, or equivalent
  • Individual:
    Private citizen
  • Public sector:
    Local, regional, federal government representative
  • Other:
    None of the above or uncertain