Ethics and research integrity. 34.1 Obligation to comply with ethical and research integrity principles
(a) ethical principles (including the highest standards of research integrity) and
(b) applicable international, EU and national law. Funding will not be granted for activities carried out outside the EU if they are prohibited in all Member States or for activities which destroy human embryos (for example, for obtaining stem cells). The beneficiary must ensure that the activities under the action have an exclusive focus on civil applications. The beneficiary must ensure that the activities under the action do not:
(a) aim at human cloning for reproductive purposes;
(b) intend to modify the genetic heritage of human beings which could make such changes heritable (with the exception of research relating to cancer treatment of the gonads, which may be financed), or
(c) intend 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. The beneficiary must respect the highest standards of research integrity — as set out, for instance, in the European Code of Conduct for Research Integrity10.
Ethics and research integrity. The Recipient must carry out the Projects in compliance with: - ethical principles (including the highest standards of research integrity) and - applicable EU, international and national law, including the Charter of Fundamental Rights of the European Union and the European Convention for the Protection of Human Rights and Fundamental Freedoms and its Supplementary Protocols. No financial support/EIT funding can be granted, within or outside the EU, for activities that are prohibited in all Member States. No financial support/EIT funding can be granted in a Member State for an activity which is forbidden in that Member State. The Recipient must pay particular attention to the principle of proportionality, the right to privacy, the right to the protection of personal data, the right to the physical and mental integrity of persons, the right to non- discrimination, the need to ensure protection of the environment and high levels of human health protection. The Recipient must ensure that the KAVA(s)/Project(s) have an exclusive focus on civil applications. The Recipient must ensure that the activities under the Projects do not: - aim at human cloning for reproductive purposes - intend to modify the genetic heritage of human beings which could make such modifications heritable (with the exception of research relating to cancer treatment of the gonads, which may be financed) - intend 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, or - lead to the destruction of human embryos (for example, for obtaining stem cells). KAVA(s)/Project(s) involving research on human embryos or human embryonic stem cells may be carried out only if KIC LE has obtained explicit approval (in writing) from the EIT. In addition, the Recipient must respect the fundamental principle of research integrity — as set out in the European Code of Conduct for Research Integrity. This implies compliance with the following principles: - reliability in ensuring the quality of research reflected in the design, the methodology, the analysis and the use of resources - honesty in developing, undertaking, reviewing, reporting and communicating research in a transparent, fair and unbiased way - respect for colleagues, research participants, society, ecosystems, cultural heritage and the environment - accountability for the research from idea to publication, for its management and organisation, for ...
Ethics and research integrity. 12.1.- The Contractor shall carry out the tasks assigned to it in the Framework Agreement and Specific Contracts in compliance with:
a) ethical principles (including the highest standards of research integrity) and
b) applicable international, EU and national law. The Contractor may not: • carry out activities in a country outside the EU, if they are prohibited in all EU Member States or • destroy human embryos. The Contractor may not carry out activities whose aim is to:
a) carry out human cloning for reproductive purposes;
b) modify the genetic heritage of human beings in such a way as could make such changes heritable (with the exception of research relating to cancer treatment of the gonads) or
c) 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. The Contractor may not carry out activities that do not focus exclusively on civil applications. The Contractor shall respect the fundamental principle of research integrity as out in the European Code of Conduct for Research Integrity. This implies compliance with the following essential principles: • reliability in ensuring the quality of research reflected in the design, the methodology, the analysis and the use of resources; • honesty in developing, undertaking, reviewing, reporting and communicating research in a transparent, fair and unbiased way; • respect for colleagues, research participants, society, ecosystems, cultural heritage and the environment; • accountability for the research from idea to publication, for its management and organisation, for training, supervision, and mentoring, and for its wider impacts. This means that beneficiaries must ensure that persons carrying out research tasks follow the good research practices and refrain from the research integrity violations described in this Code.
Ethics and research integrity. 34.1 Obligation to comply with ethical and research integrity principles
(a) ethical principles (including the highest standards of research integrity) and
(b) applicable international, EU and national law. Funding will not be granted for activities carried out outside the EU if they are prohibited in all Member States or for activities which destroy human embryos (for example, for obtaining stem cells). The beneficiaries must ensure that the activities under the action have an exclusive focus on civil applications. The beneficiaries must ensure that the activities under the action do not:
(a) aim at human cloning for reproductive purposes;
(b) intend to modify the genetic heritage of human beings which could make such changes heritable (with the exception of research relating to cancer treatment of the gonads, which may be financed), or
(c) intend 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. The beneficiaries must respect the highest standards of research integrity — as set out, for instance, in the European Code of Conduct for Research Integrity10. This implies notably compliance with the following essential principles: - honesty; - reliability; - objectivity;
Ethics and research integrity. Obligation to comply with ethical and research integrity principles
Ethics and research integrity. 14.1 The Contractor shall carry out the tasks assigned to it in the framework agreement and in the specific contracts in compliance with:
(a) ethical principles (including the highest standards of research integrity) and
(b) applicable international, EU and national law.
14.2 The Contractor may not carry out activities that are prohibited in all EU Member States in a country outside the EU (where those activities are allowed).
14.3 The Contractor may not carry out activities whose aim is to:
(a) carry out human cloning for reproductive purposes;
(b) modify the genetic heritage of human beings in such a way as could make such changes heritable (with the exception of research relating to cancer treatment of the gonads); or
(c) 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.
14.4 The Contractor may not carry out activities that do not focus exclusively on civil applications. The Contractor shall respect the highest standards of research integrity — as set out, for instance, in the European Code of Conduct for Research Integrity1. This implies notably compliance with the following essential principles: - honesty; - reliability; - objectivity;
Ethics and research integrity. 15.1. The Contractor shall carry out the tasks assigned to it in the Framework Agreement (TD11) and in the Specific Contracts (TD12, 15 and 16) in compliance with ethical principles (including the highest standards of research integrity), and applicable international, European and national law.
15.2. The Contractor shall respect the fundamental principle of research integrity, as set out in the European Code of Conduct for Research Integrity.5 This implies compliance with the following essential principles: • Reliability in ensuring the quality of research reflected in the design, the methodology, the analysis and the use of resources. • Honesty in developing, undertaking, reviewing, reporting and communicating research in a transparent, fair and unbiased way. • Respect for colleagues, research participants, society, ecosystems, cultural heritage and the environment. • Accountability for the research from idea to publication, for its management and organization, for training, supervision and mentoring, and for its wider impacts. 5 The European Code of Conduct for Research Integrity of ALLEA of 2017. xxxxx://xxx.xxxxx.xxx/wp-content/uploads/2017/05/ALLEA-European-Code-of-Conduct-for- Research-Integrity-2017.pdf
15.3. Beneficiaries must ensure that persons carrying out research tasks follow the good research practices and refrain from the research integrity violations described in the mentioned Code.
15.4. Before starting any activity that raises an ethical issue, the Contractor shall submit to the Lead Procurer a copy of: • Any ethics committee opinion required under national law and; • Any notification or authorization for activities raising ethical issues required under national law.
Ethics and research integrity. 16.1 The contractor shall carry out the tasks assigned to it in the Framework Agreement and in the specific contracts in compliance with: ● ethical principles (including the highest standards of research integrity) and ● applicable international, EU and national law. The contractor may not carry out activities that are prohibited in all EU Member States in a country outside the EU (where those activities are allowed). The contractor may not carry out activities that do not focus exclusively on civil applications. The contractor shall respect the highest standards of research integrity — as set out, for instance, in the European Code of Conduct for Research Integrity1. This implies notably compliance with the following essential principles:
(a) honesty;
(b) reliability;
(c) objectivity;
(d) impartiality;
(e) open communication;
(f) duty of care;
(g) fairness and
(h) responsibility for future science generations. This means that contractor must ensure that persons carrying out research tasks: ● present their research goals and intentions in an honest and transparent manner; ● design their research carefully and conduct it in a reliable fashion, taking its impact on society into account; ● use techniques and methodologies (including for data collection and management) that are appropriate for the field(s) concerned; ● exercise due care for the subjects of research — be they human beings, animals, the environment or cultural objects; ● ensure objectivity, accuracy and impartiality when disseminating the results; ● allow — as much as possible and taking into account the legitimate interest of the contractor — access to research data, in order to enable research to be reproduced; ● make the necessary references to their work and that of other researchers; ● refrain from practicing any form of plagiarism, data falsification or fabrication; ● avoid conflicts of interest and misrepresentation of credentials or other research misconduct.
16.2 Before starting any activity that raises an ethical issue, the contractor shall submit to the lead procurer a copy of: ● any ethics committee opinion required under national law and ● any notification or authorisation for activities raising ethical issues required under national law. 1 The European Code of Conduct for Research Integrity of ALLEA (All European Academies) and ESF (European Science Foundation) of March 2011.
Ethics and research integrity. 16.3.1 The Supplier, including its subcontractors, shall carry out the tasks assigned to it in the Framework Agreement and Specific Contracts in compliance with ethical principles (including the highest standards of research integrity) and applicable international, EU and national law.
16.3.2 The Supplier, including its subcontractors, shall carry out the activities under the Framework Agreement for non-military purposes only.
16.3.3 The Supplier may not carry out activities in a country outside the EU if they are prohibited in all EU Member States or destroy human embryos.
16.3.4 The Supplier may not carry out activities whose aim is to:
a) carry out human cloning for reproductive purposes;
b) modify the genetic heritage of human beings in such a way as could make such changes heritable (with the exception of research relating to cancer treatment of the gonads) or
c) 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.
16.3.5 The Supplier may not carry out activities that do not focus exclusively on civil applications.
16.3.6 The Supplier, including its subcontractors, shall comply with the highest standards of research integrity — as set out, for instance, in the European Code of Conduct for Research Integrity. This implies, that Supplier shall notably compliance with the following essential principles:
a) Honesty in developing, undertaking, reviewing, reporting and communicating research in a transparent, fair and unbiased way;
b) Reliability in ensuring the quality of research reflected in the design, the methodology, the analysis and the use of resources;
c) Respect for colleagues, research participants, society, ecosystems, cultural heritage and the environment;
d) Accountability for the research from idea to publication, for its management and organisation, for training, supervision and mentoring, and for its wider impacts;Objectivity;
Ethics and research integrity. 34.1 Obligation to comply with ethical and research integrity principles
(a) ethical principles (including the highest standards of research integrity) and
(b) applicable international, EU and national law. Funding will not be granted for activities carried out outside the EU if they are prohibited in all Member States or for activities which destroy human embryos (for example, for obtaining stem cells). The beneficiaries must ensure that the activities under the action have an exclusive focus on civil applications. The beneficiaries must ensure that the activities under the action do not:
(a) aim at human cloning for reproductive purposes;
(b) intend to modify the genetic heritage of human beings which could make such changes heritable (with the exception of research relating to cancer treatment of the gonads, which may be financed), or
(c) intend 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. In addition, the beneficiaries must respect the fundamental principle of research integrity — as set out, for instance, in the European Code of Conduct for Research Integrity10. This implies compliance with the following fundamental principles: - reliability in ensuring the quality of research reflected in the design, the methodology, the analysis and the use of resources; - honesty in developing, undertaking, reviewing, reporting and communicating research in a transparent, fair and unbiased way; - respect for colleagues, research participants, society, ecosystems, cultural heritage and the environment; - accountability for the research from idea to publication, for its management and organisation, for training, supervision and mentoring, and for its wider impacts and means that beneficiaries must ensure that persons carrying out research tasks follow the good research practices and refrain from the research integrity violations described in this Code. This does not change the other obligations under this Agreement or obligations under applicable international, EU or national law, all of which still apply.
