Exceptions to fully informed consent in clinical Research

K. E. Larsen; D. E. Hilleman

doi:10.3109/10601339009024025

Exceptions to fully informed consent in clinical Research

K. E. Larsen, D. E. Hilleman

Department of Pharmacy Practice

Research output: Contribution to journal › Article › peer-review

Abstract

The doctrine of informed consent is fundamental to all medical personnel involved in investigational research. Informed consent arose from the Helsinki declaration that stated, "concern for the interests of the subject must always prevail over the interests of science and society." (6) As clinical research is a part of medical practice, it is reasonable to assume that exceptions to fully informed consent that are defendable in medical practice can be applied to clinical research as well. The exceptions to fully informed consent are waiver, incompetence, therapeutic priviledge, emergency, or proxy.

Original language	English (US)
Pages (from-to)	99-112
Number of pages	14
Journal	Clinical Research and Regulatory Affairs
Volume	8
Issue number	2
DOIs	https://doi.org/10.3109/10601339009024025
State	Published - Jan 1 1990

All Science Journal Classification (ASJC) codes

Pharmacology
Pharmaceutical Science
Pharmacology (medical)

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Exceptions to fully informed consent in clinical Research

Abstract

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