General Information

European Joint Programme on Rare Diseases (EJP RD) Call for Proposals 2021

General Information – JTC 2021

 

 
 
 

European Joint Programme on Rare Diseases (EJP RD) Call for Proposals 2021

Social Sciences and Humanities Research to Improve Health Care Implementation and Everyday Life of People Living with a Rare Disease

The European Joint Programme on Rare Diseases (EJP RD) has successfully implemented two Joint Transnational Calls since 2019 to further help in coordinating the research efforts of European, Associated and non-European countries in the field of rare diseases and implement the objectives of the International Rare Disease Research Consortium (IRDiRC). These actions are following the ten Joint Transnational Calls for rare diseases research projects launched previously by the ERA-Net E-Rare since 2006.
A number of national and regional funding organisations will participate in the EJP RD Joint Transnational Call (JTC) 2021 and will fund multilateral research projects on rare diseases under the EJP-COFUND action. The following funding organisations in their respective countries/regions have expressed their interest in joining the JTC2021:

  • Austrian Science Fund (FWF), Austria
  • Research Foundation Flanders (FWO), Belgium, Flanders
  • Fund for Scientific Research – FNRS (F.R.S.-FNRS), Belgium, French-speaking community
  • Canadian Institutes of Health Research – Institute of Genetics (CIHR-IG), Canada
  • Ministry of Social Affairs of Estonia (MoSAE), Estonia
  • French National Research Agency (ANR), France
  • Federal Ministry of Education and Research (BMBF), Germany
  • National Research, Development and Innovation Office (NKFIH), Hungary
  • Chief Scientist Office of the Ministry of Health (CSO-MOH), Israel
  • Italian Ministry of Health (MoH-IT), Italy
  • Institut national de la santé et de la recherche médicale (INSERM), France
  • Tuscany Region (RT/TuscReg), Tuscany (Italy)
  • Research Council of Lithuania (LMT), Lithuania
  • National Research Fund (FNR), Luxembourg
  • National Centre for Research and Development (NCBR), Poland
  • Slovak Academy of Sciences (SAS), Slovakia
  • National Institute of Health Carlos III (ISCIII), Spain
  • Swiss National Science Foundation (SNSF), Switzerland
  • Scientific and Technological Research Council (TUBITAK), Turkey

AIM OF THE CALL

The aim of the call is to enable scientists in different countries to build an effective collaboration on a common interdisciplinary research project based on complementarities and sharing of expertise, with a clear future benefit for patients.

Topic: Social sciences and Humanities Research to improve health care implementation and everyday life of people living with a rare disease

Research proposals should cover at least one of the following areas

  • Health & social care services research to improve patient and familial/household health outcomes
  • Economic Impact of Rare diseases
  • Psychological and Social Impact of Rare diseases
  • Studies addressing the impact/burden of the delay in diagnosis and of the lack of therapeutic intervention.
  • e-Health in rare diseases: Use of innovative technology systems for care practices in health and social services
  • Development and enhancement of health outcomes research methods in rare diseases
  • Effects of pandemic crisis and the global outbreak alert and response on the rare disease field, and the emergence of innovative care pathways in this regard.

Other research topics are possible as long as they focus on SSH research and are not in the excluded topics list.

The following approaches and topics are excluded from the scope of the call:

  • Interventional clinical trials to prove efficacy of drugs, treatments, surgical procedures, medical technology procedures. This also includes studies comparing efficacy, e.g. B. two surgical techniques or therapies. Clinical phase IV pharmacovigilance studies cannot be funded either.
  • Studies on the exclusive testing of the safety of medical devices.
  • Health technology assessment reports (HTA) for a specific product.
  • Projects focusing on meta-analyses and systematic reviews.
  • Creation of new registers or establishment of new long-term cohorts and / or promotion of existing registers or long-term cohorts beyond the specific research question of the submitted project.
  • Development of new digital or technological tools.
  • Projects to accelerate diagnosis and/or explore disease progression and mechanisms of rare diseases as covered in EJP RD JTC 2019.
  • Development of new therapies as covered in EJP RD JTC 2020.
  • Projects focusing only on rare neurodegenerative diseases which are within the main focus of the Joint Programming Initiative on Neurodegenerative Disease Research (JPND). These are: Alzheimer’s disease and other dementias; Parkinson’s disease (PD) and PD-related disorders; Prion diseases; Motor Neuron Diseases; Huntington’s disease; Spinal Muscular Atrophy and dominant forms of Spinocerebellar Ataxia. Interested researchers should refer to the relevant JPND calls. Childhood dementias/neurodegenerative diseases are not excluded.
  • Rare infectious diseases, rare cancers and rare adverse drug events in treatments of common diseases.

Type of studies

  • Qualitative Analysis  

Description and analysis of patient’s lifepath,  as well as healthcare and social care processes and structures, using qualitative methods, form an important part of SSH research. Qualitative studies are often the starting point for identifying relevant questions for further quantitative studies. The projects can also include further development of scientific instruments and methods and their validation in practice. The sole translation, evaluation and/or testing of individual questionnaires is not funded. 

  • Non-interventional quantitative studies 

In order to be able to name the strengths and weaknesses of a system, in a scientifically sound manner, the collection and evaluation of relevant and valid data using recognized methods and procedures are necessary, as well as the further development and validation of scientific instruments and methods. Adequate comparison groups are essential. In this type of studies, the system is preferably analyzed prospectively.  This includes observational studies like anthropological studies, case control studies, cross-sectional and longitudinal studies as well as cost-effectiveness studies.

  • Interventional studies on care implementation

These are comparative interventional studies to evaluate the effectiveness of practices under everyday conditions. The study design must be multi-armed. Structural equality of the groups can be achieved through suitable measures, e.g. by randomization. In contrast to clinical studies that show the efficacy of a therapeutic measure, e.g. test a drug, the interventional studies funded within the scope of this Call require proof of effectiveness and the effect of measures in everyday care e.g. in heterogeneous patient groups examined. This requires the use of patient-relevant endpoints, e.g. health-related quality of life, as the primary targets of the studies. Other methodological prerequisites for an interventional study on care implementation include broad inclusion and exclusion criteria, if possible, no requirements for the patients going beyond everyday care and the conduct of the study in the facilities in which the examined intervention is used as part of regular practices. Project proposals must clearly demonstrate the potential health impact as well as the added value of transnational collaboration. This includes participatory action research. For interventional studies on care implementation, feasibility must be clearly demonstrated regarding the 3 years duration of the project, including realistic timelines for regulatory aspects like ethical approval etc. in different countries.

 

CONSORTIUM MAKEUP

Projects shall involve a group of rare diseases or a single rare disease following the European definition i.e. a disease affecting not more than five in 10.000 persons in the European Community, EC associated states and Canada. Applicants are encouraged to assemble groups of rare diseases based on solid criteria and commonalities if these leverages added value in sharing resources or expertise and has the capacity to elucidate common disease mechanisms and therapeutic targets.

Partners belonging to one of the following categories may request funding under a joint research proposal (according to country/regional regulations):

  • Academia (research teams working in universities, other higher education institutions or research institutes),
  • Clinical/public health sector (research teams working in hospitals/public health and/or other health care settings and health organizations),
  • Enterprises (all sizes of private companies) when allowed by national/regional regulations,
  • Patient advocacy organizations.

The maximum duration of the project is three years.

Only transnational projects will be funded. Each consortium submitting a proposal must involve three to six eligible principal investigator partners from at least three different participating countries. No more than two eligible partners from the same country can be present in each consortium (further national limits may apply). This limit applies to Early Career Researchers and partners from underrepresented countries (see below). PAOs requesting funding do not count toward this total.

The number of partners can be increased to 8 in two cases:

  • The inclusion of partners from participating countries usually underrepresented in projects (Czech Republic, Slovakia, Hungary, Lithuania, Poland, and Turkey).
  • The inclusion of Early Career Researchers as full partners.

The aim of this call is to support multinational, innovative, and multidisciplinary humanities and social sciences research projects to improve healthcare implementation and everyday life of people living with a rare disease.
Consortia have to include both SSH and clinical expertise in their consortium. Moreover, to ensure that the needs and priorities of rare disease patients are adequately addressed, they or their representatives must be appropriately involved in all projects.

Our matchmaking tool will help you find your ideal project partner.

PRELIMINARY TIMETABLE

There will be a two-stage submission procedure for joint applications: pre-proposals and full proposals. 
An independent international Scientific Evaluation Committee will carry out a scientific evaluation according to specific evaluation criteria.

16th February 2021: Pre-proposal submission deadline

End of April 2021: Invitation to full proposal

15th June 2021: Full proposal submission deadline

30th July 2021: Deadline for rebuttals

November 2021: Notification of funding decision

CONTACT 

For general questions regarding the joint call please contact the Joint Call Secretariat at the FFRD, France: JTC2021@ejprarediseases.org

Diana Désir-Parseille
diana.desir-parseille@fondation-maladiesrares.com
+33 (0) 1 58 14 22 81

Laura Benkemoun
laura.benkemoun@fondation-maladiesrares.com

For questions regarding national eligibility criteria and requirements please contact the national contact person listed below

ADDITIONAL INFORMATION

Documents 

Matchmaking tool

NATIONAL CONTACT POINTS

Country/RegionFunding OrganisationContact Details
AustriaAustrian Science Fund (FWF)
www.fwf.ac.at
Stephanie Resch
+43 (1) 505 67 40-8201
stephanie.resch@fwf.ac.at
BelgiumThe Research Foundation – Flanders (FWO) Toon Monbaliu
eranet@fwo.be
+32 (0)2 550 15 70
Belgium
The Fund for Scientific Research – FNRS (F.R.S.-FNRS)
Dr. Florence Quist
Florence.quist@frs-fnrs.be
+32 (0)2 504 9351
CanadaCanadian Institutes of Health Research
Institute of Genetics (CIHR-IG)
www.cihr-irsc.gc.ca
Jennifer Vineham
jennifer.vineham@cihr-irsc.gc.ca
+1 343-552-2760
Czech RepublicMinistry of Education, Youth and Sports (MEYS)
www.msmt.cz
Judita Klosaková (MSMT)
+420 234 811 504
Judita.Klosakova@msmt.cz
FranceThe French National Agency for Research – ANRDr. Florence Guillot
florence.guillot@anr.fr
EJPRDcall@anr.fr
Germany
Federal Ministry of Education and Research (BMBF) / Project Management Agency of the German Aerospace Centre (BMBF/ PT-DLR)
www.gesundheitsforschung-bmbf.de/
Dr. Katarzyna Saedler
Dr. Michaela Fersch
Dr. Ralph Schuster

+49228-38212453
SelteneErkrankungen@dlr.de
Hungary
National Research, Development and Innovation Office (NKFIH)
www.nkfih.gov.hu
Előd Nemerkényi
+36 1 8963987
elod.nemerkenyi@nkfih.gov.hu
Israel
Chief Scientist Office – Israeli Ministry of Health (CSO-MOH)
Dr. Irit Allon
+972-2-5082167
IRIT.ALLON@moh.gov.il
ItalyItalian Ministry of Health (MoH-IT)
www.salute.gov.it
Maria Grazia Mancini
mg.mancini-esterno@sanita.it

Dr. Monica Paganelli
+39 06 5994 2408
m.paganelli@sanita.it
ItalyMinistry of Education, Universities and Research (MIUR)
www.ricercainter nazionale.miur.it/
Aldo Covello
+39 06.5849.6465
aldo.covello@miur.it

Maria Bianco
+39 06.5849.7146
maria.bianco@miur.it
Italy (Tuscany)Tuscany Region (RT/TuscReg)
www.regione.toscana.it
Donatella Tanini
+39 055 4383256

Teresa Vieri
+39 055 4383289
ejprare@regione.toscana.it
LithuaniaResearch Council of LithuaniaDr. Živilė Ruželė
+370 676 14383
zivile.ruzele@lmt.lt
LuxembourgLuxembourg National Research Fund Dr. Sean Sapcariu
+352 691 362 831
sean.sapcariu@fnr.lu
Poland
National Centre for Research and Development (NCBR)
www.ncbr.gov.pl/en/
Marcin Chmielewski
+48 22 39 07 109
marcin.chmielewski@ncbr.gov.pl
SlovakiaSlovak Academy of Sciences Dr. Zuzana Cernakova
+421 (0) 2 5751 0 118
Cernakova@up.upsav.sk
SpainNational Institute of Health Carlos IIIClara Martín
+34 91822 2567
c.martin@isciii.es
SwitzerlandSwiss National Science Foundation
Dr. Florence Ettlin
+41 31 308 21 87
florence.ettlin@snf.ch
TurkeyThe Scientific and Technological Research Council of Turkey (TUBITAK) Dr. Jale Sahin
+90(312)298 1796
EJPRD@tubitak.gov.tr

1st EJP RD Joint Transnational Call for Rare Diseases Research Project (JTC 2019)

The submissions of pre-proposals are now CLOSED.

For more information please download and read all related call documents under the  Funding “Documents” section.

It is strongly recommended to contact your National Contact Person (list of contacts is provided under Funding  “National Contact Points” section or in Guidelines for applicants documents).

Please note that some national/regional funders operate an additional eligibility check that must be performed BEFORE the submission of the proposal – you will find all details in the Guidelines and (if relevant) dedicated pre-submission forms in the Documents section.

Research consortia who intend to submit a transnational project proposal should register at the electronic proposal system as soon as possible via the link: https://ptoutline.eu/app/ejprd19

The E-Rare ERA-Net has successfully implemented ten Joint Transnational Calls for rare disease research projects since 2006. This effort is now continued in the frame of the European Joint Programme on Rare Diseases (EJP RD) that has been established to further help in coordinating the research efforts of European, Associated and non-European countries in the field of rare diseases and implement the objectives of the International Rare Disease Research Consortium (IRDiRC).

The following funding organisations:
* Austrian Science Fund (FWF), Austria
* Research Foundation Flanders (FWO), Belgium, Flanders
* Fund for Scientific Research – FNRS (F.R.S.-FNRS), Belgium, Wallonia
* Canadian Institutes of Health Research – Institute of Genetics (CIHR-IG), Canada
* Fonds de recherche du Québec-Santé (FRQS), Québec (Canada)
* Ministry of Education, Youth and Sports (MEYS), Czech Republic
* Ministry of Social Affairs of Estonia (MoSAE), Estonia
* Academy of Finland (AKA), Finland
* French National Research Agency (ANR), France
* French Foundation for Rare Diseases (FFRD), France
* Federal Ministry of Education and Research (BMBF), Germany
* German Research Foundation (DFG), Germany
* General Secretariat for Research and Technology (GSRT), Greece
* National Research, Development and Innovation Office (NKFIH), Hungary
* Health Research Board, (HRB), Ireland
* Chief Scientist Office of the Ministry of Health (CSO-MOH), Israel
* Italian Ministry of Health (MoH-IT), Italy
* Ministry of Education, Universities and Research (MIUR), Italy
* Regional Foundation for Biomedical Research (FRRB), Lombardy (Italy)
* Tuscany Region (RT/TuscReg), Tuscany (Italy)
* Research Council of Lithuania (RCL), Lithuania
* National Research Fund (FNR), Luxembourg
* National Centre for Research and Development (NCBR), Poland
* The Foundation for Science and Technology (FCT), Portugal
* Slovak Academy of Sciences (SAS), Slovakia
* National Institute of Health Carlos III (ISCIII), Spain
* Swedish Research Council (SRC), Sweden
* Vinnova, Sweden
* Swiss National Science Foundation (SNSF), Switzerland
* Netherlands Organization for Health Research and Development (ZonMw), The Netherlands
* The Scientific and Technological Research Council of Turkey (TUBITAK), Turkey
* The French National Institute of Health and Medical Research (INSERM), France (will provide dedicated funding only to Patient Advocacy Organisations),

intend to open the first EJP RD Joint Transnational Call (JTC 2019) for funding multilateral research projects on rare diseases together with the European Commission (EC) under the EJP-COFUND mechanism. The call is expected to be opened simultaneously by the above-mentioned funding organisations in their respective countries/regions.

Aim and Topics

The aim of the call is to enable scientists in different countries to build an effective collaboration on a common interdisciplinary research project based on complementarities and sharing of expertise, with a clear benefit for patients.

Topic: Research projects to accelerate diagnosis and/or explore disease progression and mechanisms of rare diseases

Transnational research proposals must cover at least one of the following areas, which are equal in relevance for this call:

Research to accelerate diagnosis, e.g:

* New schemes for finding diagnosis for undiagnosed patients;

* Improved annotation and interpretation of variants and development of diagnostic tests for the more prevalent variants;

* Novel modalities of functional analysis of candidate variants through in vitro, cell, tissue or animal studies;

* Omic or multi-omic integrated approaches for discovery of disease causes and mechanisms including development of relevant bioinformatic tools.

Research to explore disease progression and mechanisms, e.g:

* Natural history studies and patient registries (also for clinical trial readiness). Whenever possible these should include development and use of patient reported outcome measures. In addition, the exploration of the use of standardized M-Health-based surveillance instruments and of patient entered data to gather information for natural history studies is welcome;

* Identification of clinical biomarkers, clinical outcome measures and surrogate endpoints;

* Identification of novel pathophysiological pathways in appropriate disease models that effectively mimic the human condition.

Furthermore, additional elements need to be considered in the application:

* The design of the study (sample collection, statistical power, interpretation, relevant models for hypothesis validation) must be well justified and has to be part of the proposal;

* For natural history studies and patient registries: strategies and timelines for patient recruitment, retention, assessment, and analysis must be included. Data supporting the proposed recruitment numbers is mandatory. The study design and objectives should take into consideration what information regarding the rare disease population would be needed in order to pursue clinical trials or other health care related studies in that rare disease. There always need to be clear research questions that are addressed in the study/registry. Clear plans for sustainability of the resources must be described. Consideration of common data elements as outlined in the recent publication “Set of Common Data Elements for RD Registration” is highly recommended;

* Appropriate bioinformatics and statistical skills should constitute, whenever justified, an integral part of the proposal, and the relevant personnel should be clearly specified;

* The new research data resulting from the project should be treated permissible according to the FAIR principles (for more information: see “The FAIR Guiding Principles for scientific data management and stewardship”, and deposited and shared, according to the national/regional rules of the countries involved. It is strongly advised to make data accessible through RD-Connect (connecting databases, patient registries, biobanks and clinical bioinformatics data into a central resource for researchers worldwide) and through Elixir (compiling a list of resources for the deposition of experimental, biomolecular data). To make research data findable, accessible, interoperable and re-usable (FAIR), a data management strategy for the proposed full project is mandatory in the full proposal stage. Some countries involved in EJP RD JTC 2019 will also ask for a data management plan (DMP) at national level at the stage of full proposal or after granting of the project;

* To ensure that the needs and priorities of rare disease patients are adequately addressed, they or their representatives should be appropriately involved in all projects wherever relevant. For examples, inclusion and involvement of patient representatives includes but is not restricted to natural history studies / registries where patients should be involved in the governance of the registry. Please consult the INVOLVE website for information on various ways to involve patients. For additional guidance and practical advice on patient involvement in research studies, please consult also the JPND guidelines.

The following approaches and topics are excluded from the scope of this call:

* Approaches concerning rare infectious diseases or rare cancers;

* Approaches concerning rare adverse drug events/medical complications in treatments of common diseases;

* Studies that focus on pre-clinical therapy development and/or validation in cellular or animal models. These will be addressed in future calls;

* Interventional clinical trials;

* Rare neurodegenerative diseases which are within the main focus of the Joint Programming Initiative on Neurodegenerative Disease Research JPND. These concern: Alzheimer’s disease and other dementias; Parkinson’s disease (PD) and PD-related disorders; Prion disease; Motor Neuron Diseases; Huntington’s disease; Spinal Muscular Atrophy and dominant forms of Spinocerebellar Ataxia. Interested researchers should refer to the relevant JPND calls. Not excluded through this specification are childhood dementias/neurodegenerative diseases.

Projects shall involve a group of rare diseases or a single rare disease following the European definition i.e. a disease affecting not more than five in 10.000 persons in the European Community, EC associated states and Canada. Applicants are encouraged to assemble groups of rare diseases based on solid criteria and commonalities if this leverages added value in sharing resources or expertise and has the capacity to elucidate common disease mechanisms and therapeutic targets.

The research projects submitted within this call must be based on novel ideas stemming from consolidated previous results or preliminary data and must be clearly endowed with benefit for the patients, i.e. studies allowing a rapid implementation into public health-related decisions or into the clinics. To achieve this goal, the necessary expertise and resources should be brought together from academia, clinical/public health sector and private companies whenever relevant. The research teams within a consortium should include investigators from complementary scientific disciplines, research areas and expertise necessary to achieve the proposed objectives.

The research proposals must demonstrate complementary and synergistic interaction among the partner teams. There should be clear added value in the transnational collaboration over the individual projects, in terms of:

1. Gathering a critical mass of subjects/patients and or subjects/patients databases and corresponding biological materials that would not be possible otherwise;

2. Sharing of resources (biobanks, models, databases, diagnostic tools, etc.), of specific know-how and/or innovative technologies including “-omics”, and of expertise. The projects should clearly demonstrate the potential health impact.

General conditions for application

Joint research proposals may be submitted by applicants belonging to one of the following categories (according to country/regional regulations):

* academia (research teams working in universities, other higher education institutions or research institutes)

* clinical/public health sector (research teams working in hospitals/public health and/or other health care settings and health organisations)

* enterprise (all sizes of private companies). Participation of small and medium-size enterprises (SMEs) is encouraged when allowed by national/regional regulations

* patient advocacy organisations (PAOs – see more information below and refer to the INSERM contact point) .

Please note that the inclusion of a non-eligible research partner (principle investigator) in a proposal leads to the rejection of the entire proposal without further review. Whilst applications will be submitted jointly by applicants from several countries/regions, individual groups will be funded by the individual funding organisation of their country/region that is participating in the EJPRD JTC 2019. The applications are therefore subjected to eligibility criteria of individual funding organisations. Applicants are strongly advised to contact their corresponding national/regional representative and confirm eligibility with their respective funding organisations in advance of submitting an application (see national/regional contact details).

Only transnational projects will be funded. Each consortium submitting a proposal must involve a minimum of four eligible and a maximum of six eligible research partners from at least four different countries participating to the call (see list above).

No more than two eligible research partners from the same country participating in the call will be accepted in one consortium.

The Joint Call Secretariat and national/regional funding organisations will perform cross-checks in parallel submissions to other joint transnational calls (e.g. NEURON, JPND, EuroNanoMed, ERA PerMed and others) and national calls. Applicants shall avoid applying for same research activities to different calls. Double funding is not allowed.

The consortium coordinator must always be eligible to receive funding from the funding organisations participating in the call and cannot be a partner that joins only with their own funding. Only groups that contribute substantially to at least one of the work packages are considered as partners and should be indicated in the project.

Applicants are encouraged to include research partners from participating countries usually underrepresented in projects (Czech Republic, Slovakia, Estonia, Hungary, Lithuania, Poland, and Turkey). If they include such research partners, the maximum number of research partners can be increased to eight (see tables below).

Consortia are also encouraged to include Early Career Scientists as principal investigators in their proposal. Early career PIs must prove that they are scientifically excellent and independent, for example that they lead or have led a research group or project. They also must clearly be eligible according to national/regional funding regulations. Early Career Scientists should be clearly identified in the proposal and their CV.

Additional research partners that secure their own funding may join consortia. However, their number is limited to two and depends on the number of research partners requesting funding (see table below). These additional research partners can only come from countries that are not involved in the EJPRD JTC 2019 funding or are not eligible for the respective funding organization due to national/regional rules. These research partners must state clearly in the proposal if these funds are already secured or if not, how they plan to obtain funding in advance of the project start, as well as what the concrete amount of contributed funding will be. It will be required to document the availability of their funds before October 1, 2019. In the (pre)proposal form these research partners are mentioned in the category «Associated research partners not asking for funding».

Number of research partners requesting national/regional funding

Possible number of additional research partners with own funding

4

2

5

6

7

(only possible with inclusion of 1 partner from usually underrepresented countries)

1

8

(only possible with inclusion of 2 partners from usually underrepresented countries)

0

 

To collect the necessary patient data and/or samples for the proposed study, a consortium may need to collaborate with other centres. If the unique role of those centres is providing patients data and/or samples for the study only, they will not be considered as research partners of the consortium but can be included otherwise, e.g. via cooperation agreements or subcontracting.

In addition, the inclusion of patient advocacy organizations (PAO) in the proposal is highly encouraged. These can be involved in all levels of the proposed work including helping to develop the research question or patient centred tools, advising on prioritisation, being involved in advisory groups, being a member of the consortium steering group or the governance group of a registry, carrying out the research and disseminating the research findings. Therefore PAOs are also eligible to receive funding for their activities. If PAO involvement is not deemed appropriate within a specific research study, this should be explained and justified. The included PAO(s) will not be counted as a national/regional principal investigator research partner and therefore their inclusion does not influence the maximum number of research partners as described above.

Timetable

There will be a two-stage submission procedure for joint applications: pre-proposals and full proposals.

The call is scheduled to open on December 15, 2018.

The deadline for submitting the pre-proposals is February 15, 2019.

An independent international Scientific Evaluation Committee will carry out a scientific evaluation according to specific evaluation criteria. Based on this central evaluation, selected consortia will be invited to submit a full proposal by early May 2019 (indicative deadline for full proposals: June 11, 2019).

Joint Call Secretariat Contact:

Dr. Katarzyna Saedler
+49 (0)228 3821 1947
katarzyna.saedler(at)dlr.de

Dr. Michaela Fersch
+ 49 228 3821 1268
michaela.fersch(at)dlr.de

Dr. Ralph Schuster
+ 49 228 3821 1233
ralph.schuster(at)dlr.de

For questions regarding national eligibility criteria and requirements please contact the national contact person in your country – list available HERE