Informed consent form

Author:Prof. Dr. med. Peter Altmeyer

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Last updated on: 29.10.2020

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ICF

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DefinitionThis section has been translated automatically.

Before voluntary participation in a clinical trial, the trial participant (patient or test person) must give written consent or consent (Informed Consent Form - ICF) according to § 40 AMG, § 20 MPG, § 3 (2b) of the GCP regulation and the Declaration of Helsinki.

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Last updated on: 29.10.2020