Open Call for Transnational Service Provision

Under the canSERV Open Call researchers are welcome to apply to a portfolio of services offered by canSERV to address the research needs of the entire oncology developmental pipeline.


Submission Deadline:
31st August 2023, 2:00pm CEST

Your research project

  • Can vary from basic discovery science to translational science and translation into personalised oncology.
  • Is expected to address at least one of the four strategic goals of the Cancer Mission [1] (understanding of cancer; prevention and early detection; diagnosis and treatment; quality of life for patients and their families).

If granted, you will benefit from:

  • Free of charge access to canSERV service(s) (equipment, expertise, resources) offered by the canSERV consortium.
  • Transnational services comprising the following fields: disease models, advanced cutting-edge technologies, biomarkers research and development, novel therapeutics developments, complex clinical trial design and support, personalised oncology implementation pipelines and recommendations, and regulatory support and tools to analyse the socioeconomic dimension of research activities. A detailed service list is available in the canSERV Service Catalogue.

For this Call, you should:

  • Select the service(s) you would like to have access to from the Catalogue.
  • Choose only services that are provided in a different country where you, or most of your research group, are based.
  • Agree that data generated from the chosen services will comply with FAIR principles (findable, accessible, interoperable, and reusable). This will enable rapid execution of cross-European federated analyses of cancer-related data.

The indicative overall budget for this call is EUR 1.000.000, which can be increased in the event of many successful applications.

The Call is planned to remain open until 31 August 2023, 2pm CEST.

Similar open calls are planned for the next two years as long as funds are available.


Applications are continuously evaluated over this period. Evaluation takes 4-10 weeks, based on the complexity of the services requested. Once an application is submitted, we will communicate to you the estimated time for the final decision. The evaluation criteria is based on excellence, impact, and quality of the submitted proposal.

How do you gain access to your services?

All communication is conducted through our easy-to-use platform: the canSERV Common Access Management System (CAMS link).

1. Selection: Enter CAMS, and select the services you are interested in.

2. Negotiation: As soon as you submit the selected services, our transnational access (TNA) manager will contact you to clarify the required details and to communicate how and when the service could be provided.

3. Submission: After the negotiation step, you will be asked to fill in and submit our short application form describing your research proposal.

4. Evaluation: An independent review panel (IRP) will evaluate submitted applications. The final decision will be taken by the canSERV Scientific and Management Board for approval or rejection based on the IRP evaluation outcome and available budget.

5. Service provision: If approved, the service provision may start either immediately or as agreed with the service provider/TNA manager. Enquiries related to your application and the offered services can be addressed any time during your application using (please add subject: “first open call”).

Transnational Access

What is Transnational Access (TNA)?

Transnational Access allows researchers (users, applicants) free of charge access to services (equipment, expertise, resources) offered by the canSERV consortium members. 

Transnational access can be:

  • In person (physical access), with users visiting the research infrastructure facility/installation and receiving the service “hands-on”.
  • Remotely (remote access), with research infrastructure resources and services offered online/remotely.

This opportunity is open to all European and non-European researchers. Scientists can only apply for TNA services outside the country of their home institute.
There is an exception when access is provided by an international organisation, the Joint Research Centre (JRC), ERICs or similar legal entities with international membership. If you select services from such entities, please contact us to clarify the exception rule.



Applications can be submitted by those individuals or organisations, who meet ALL the following criteria:

Who can apply?

Researchers, including junior and senior individual researchers, academic institutes, biotech/pharmaceutical SMEs, also groups of scientists, networks and consortia from public and private entities in European and non-European countries.


Applicants must be affiliated with an organisation in or outside the European Union.


This grant only supports TNA as described above in point one.


Results and/or data obtained from using the services provided under the canSERV Open Call must comply with the FAIR principles and might be shared initially with other ongoing initiatives within the EU Cancer Mission, EOSC4Cancer and, when established,, for the development and improvement of further services. Furthermore, the results and/or data will be reused within the canSERV project or other EU Cancer Mission initiatives at a certain time after service provision according to the canSERV user agreement. The data generated will then be included in the canSERV service list to support the canSERV Catalogue of Open Digital Research Services. If the results and/or data are published, canSERV must be acknowledged in publications. Only user groups that are allowed to disseminate the results they have generated may be eligible for access (unless the users are working for SMEs).


Evaluation criteria

Scientific evaluation will take into consideration the following three criteria:

  • Scientific merit and/or clinical impact of the research proposal
  • Justification to the solicited service
  • Feasibility of the proposal

Based on the evaluation outcome, the final decision will be taken by the Scientific Management Board of canSERV. Applicants will be informed within max. 12 weeks after the submission deadline if their submitted proposal has been accepted.

Please read the Terms & Conditions (for us)

For more information on our canSERV partner, please visit Partners.

Information about the Call, proposal submission and evaluation is available on request from

Catalogue of Services

Disease Models

Field 1 - Disease Models

These models range from state-of-the-art in vitro models like 3D cultures, organoids and organs-on-a-chip towards in vivo, patient-proximate models and advanced precision cancer models generated using CRISPR-Cas9.

Advanced technologies for Personalised Oncology

Field 2 - Advanced technologies for Personalised Oncology

These services provide the cancer research community with access to cutting-edge services and technologies, as well as the associated expertise in their use, to address cancer research questions at a molecular, cellular and whole organism level. 


Field 3 - Biomarker research, development, and validation

These services will provide access to cutting-edge and high-quality services (e.g., liquid biopsies, imaging biomarkers including radiomics, microbiomics, omics signatures, etc.) that will support the optimization of existing screening programmes, the advancement of novel approaches for screening and early detection, identification of new biomarker sets, as well as will contribute to the development of novel therapeutics based on molecular predictors. 

New Therapeutics

Field 4 - New Therapeutic solutions

These services will provide access to a wide range of state-of-the-art services aiming to facilitate the development of novel therapeutic solutions for innovative personalised cancer research, as well as facilitate both clinical and translational research studies with focus mainly on: a) incorporate Small Molecules and Screening and b) Advanced Therapies and Biologicals Development Services.

Translation into Personalised Oncology Clinical Practice

Field 5 - Accelerated Translation into Personalised Oncology Clinical Practice

These services are specifically aimed at providing expert advice even to a single complex patient case or to a related finding or new discovery, so that patients can benefit from the results of cancer research possibly before the lengthy process of prospective clinical trials is completed. 

Digital Research Services

Field 6 - Open Digital Research Services

These services aim to combine the complex landscape of reusable biomedical data and analytic tools in the context of tumour biology complexity, in order to provide unprecedented opportunities for the cancer community for the development of novel techniques and understanding of the impact of cancer diagnostics and treatment from a molecular to a population level. 

Public health measures

Field 7 - Access to human samples and data

These services facilitate access to human biological samples and data. This will include provision of a) retrospective and on demand collections of high-quality biological material; b) high-quality associated data (i.e., OMICS, and clinical image data); and c) scientific advice on setting up state-of-the art related translational cancer research projects. 

Clinical Trials

Field 8 - Clinical trials and design

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Field 9 - ELSI services

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