Community Research and Development Information Service - CORDIS


Guidance For Applicants. Informed Consent

Funded under: FP7


For the purposes of the Ethics Review process, the definition of Informed Consent given in the Directive 2001/20/EC relating to the implementation of good clinical practice in the conduct of clinical trials on medicinal products for human use is adopted. The principle of "informed and free decision" remains valid for any other kind of research.

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