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Ethics

The Ethics Section contains:

  • Documents to facilitate ethical review by local ethics committees
  • Roadmap: guidance on ethical and legal aspects in human biomarker research
  • Handling of ethical aspects within NewGeneris: project organization
  • What should be in a standard informed consent form?  
  • List of relevant legislation  

 

Documents to facilitate ethical review by local ethics committee

1. Summary on the handling of ethical and legal aspects within NewGeneris

This document gives a clear overview on the handling of socio-ethical and legal aspects of research on the development and use of human biomarkers in the context of the NewGeneris Integrated Project, in order to facilitate the ethical review procedures by national or domestic ethics committees throughout Europe.

Summary document[.doc]

 2. Ethics/Data protection approvals from the NewGeneris cohorts and research

The Danish National Birth Cohort

Approval from the Danish Data Protection Agency [.doc]

Informed consent form[.doc]

Information sheet[.doc]

Born in Bradford

BIB Ethical approval[.doc]

Informed consent form[.doc]

Information sheet[.doc]

INMA

INMA Ethical approval[.doc]

INMA Ethical approval-english[.doc]

Informed consent form[.doc]

RHEA

RHEA Ethical approval[.doc]

Informed consent form[.doc]

Norwegian Mother and Child Cohort

Approval Data Protection Agency[.doc]

Ethical approval[.doc]

Approval from the Directorate for Health and Social Affairs[.doc]

Informed consent form[.doc]

Information sheet[.doc]

Karolinska Institute

Ethical Approval[.doc]

WP3 - Bradford - Crete

Ethical Approval Crete

Translation of Ethical approval Crete

Approval Letter Leeds

information sheet

informed consent form

Roadmap: guidance on ethical and legal aspects in human biomarker research

The roadmap has been developped within the scope of ECNIS NoE and will be available soon.

Roadmap[.doc]

Handling of ethical aspects within NewGeneris: project organization

Ethical and legal aspects within NewGeneris[.doc]

What should be in a standard informed consent form?

Template informed consent form[.doc]

List of relevant legislation

List of legislation[.doc]

 

 By the KUL team: Ludwine Casteleyn, Birgit Dumez and Karel Van Damme