Guidance For Applicants. Informed ConsentFunded 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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Record Number: 10101 / Last updated on: 2009-01-05