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Home » Who can apply and how? (first call version) » Ethics

Ethical Checklist

RBUCE-UP / Ethical check list

Areas Excluded From Funding Under FP7 and from RBUCE-UP funding [1]

 

(i)     Research activity aiming at human cloning for reproductive purposes

 

(ii)   Research activity intended to modify the genetic heritage of human beings which could make such changes heritable (Research relating to cancer treatment of the gonads can be financed)

 

(iii)  Research activities intended to create human embryos solely for the purpose of research or for the purpose of stem cell procurement, including by means of somatic cell nuclear transfer.

 

 

Dual Use

NO

YES

Does the proposal deal with research having potential military/terrorist application ?

 

 

Does the proposal deal with research having the potential for terrorist abuse ?

 

 

For more information, please download the Cordis document Ethics/Dual Use

Privacy

NO

YES

Does the proposal involve processing of genetic information or personal data (eg. health, sexual lifestyle, ethnicity, political opinion, religious or philosophical convinction) ?

 

 

Does the proposal involve tracking the location or observation of people?

 

 

For more information, please download the Cordis document: Ethics/Privacy

Research Involving Developing Countries

NO

YES

Does the proposal involve using local resources (genetic, animal, plant, etc…) ?

 

 

Does the proposal benefit to local community (capacity building, i.e. access to healthcare, education, etc…) ?

 

 

For more information, please download the Cordis document: Ethics/DC

Informed Consent

NO

YES

Does the proposal involve children ?

 

 

Does the proposal involve patients or persons not able to give consent ?

 

 

Does the proposal involve adult healthy volunteers ?

 

 

Does the proposal involve Human Genetic Material ?

 

 

Does the proposal involve Human biological samples ?

 

 

Does the proposal involve Human data collection ?

 

 

For more information, please download the Cordis document: Ethics/Informed consent

Research on Human embryos/foetus

NO

YES

Does the proposal involve Human Embryos ?

 

 

Does the proposal involve Human Foetal Tissue/Cells ?

 

 

Does the proposal involve Human Embryonic Stem Cells ?

 

 

Does the proposal on Human Embryonic Stem Cells involve cells in culture ?

 

 

Does the proposal involve the derivation of cells from Human Embryonic Stem Cells?

 

 

For more information, please download the Cordis document : Ethics/Embryos

Research on Animals

NO

YES

Does the proposal involve animals ?

 

 

Does the proposal involve transgenic small laboratory animals ?

 

 

Does the proposal involve transgenic farm animals ?

 

 

Does the proposal involve cloning farm animals ?

 

 

Does the proposal involve non-human primates ?

 

 

For more information, please download the Cordis document : Ethics/Animals

Research on ICT implants

NO

YES

Does the proposal involve clinical trials of ICT implants ?

 

 

Research on ICT and bio/nano-electronics

NO

YES

Does the proposal involve clinical trials of ICT implants ?

 

 

For more information, please download the Cordis document: Ethics/ICT

Other ethical issues

NO

YES

Are there OTHER activities that may raise Ethical Issues ?

 

 

If YES, please specify

 

 

 

 

 

It will be asked to applicants and the Host laboratory answering YES to any of these questions to develop and explain how ethical issues at stake will be handled in the course of his/her project in the appropriate heading of the application form. The applicant shall in this appropriate heading :

- Describe the potential ethical aspects of the proposed research regarding its objectives, the methodology and the potential implications of its results;
- Justify the design of the research project from an ethical viewpoint;
- Explain how the ethical requirements set out in the work programme will be fulfilled;
- Indicate how the proposal meets the national legal and ethical requirements of the country where the research is planned to be performed;
- Indicate the timeframe for applying for opinion and/or for approval by any relevant authority at national level (such as the data protection authority, the clinical trials authority etc.).


Specific procedural modalities for research activities involving human embryonic stem cells 2] Assessment of the project:

- Advance in scientific knowledge in basic research;

- Increase in medical knowledge for the development of diagnostic, preventive or therapeutic methods to be applied to humans;

- is the use of hESC is necessary in order to achieve the scientific objectives set forth in the proposal

 

Applicants and Host laboratory will be asked to provide UniverSud Paris with all proper authorizations by the local/national ethical committees or competent authority within 3 months after the publishing of the list of selected candidates/proposals. Failure by applicant to provide said authorizations within this delay will be deemed as not accepting the fellowship.

 



[1] Art. 6 – Decision N°1982/2006/EC of 18 December 2006, JOEU 30.12.2006, L412/1

 

[2] Rules for submission of proposals, and the related evaluation, selection and award procedures, Version 3, 21 August 2008 COM (2008) 4617, Annex A

 

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