Declaration of consent

Author: Prof. Dr. med. Peter Altmeyer

All authors of this article

Last updated on: 29.10.2020

Dieser Artikel auf Deutsch

Definition
This 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.

Authors

Last updated on: 29.10.2020

Articlecontent