Informed Consent
Reference work entry
DOI: https://doi.org/10.1007/3-540-29623-9_7497
Definition
Informed consent of patients and probands is an essential moral, regulatory, and legal prerequisite for medical examination and treatment, as well as in clinical research; researchers are morally and legally obligated to inform adequately and to seek consent without pressure or promises; patients and probands must be given the right to ask for termination of treatment or involvement in research.
Copyright information
© Springer-Verlag 2006