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 |
|---|---|
| Pages (from-to) | 99-112 |
| Number of pages | 14 |
| Journal | Clinical Research and Regulatory Affairs |
| Volume | 8 |
| Issue number | 2 |
| DOIs | |
| State | Published - 1990 |
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All Science Journal Classification (ASJC) codes
- Pharmaceutical Science
- Pharmacology
- Pharmacology (medical)
Cite this
Exceptions to fully informed consent in clinical Research. / Larsen, K. E.; Hilleman, Daniel E.
In: Clinical Research and Regulatory Affairs, Vol. 8, No. 2, 1990, p. 99-112.Research output: Contribution to journal › Article
}
TY - JOUR
T1 - Exceptions to fully informed consent in clinical Research
AU - Larsen, K. E.
AU - Hilleman, Daniel E.
PY - 1990
Y1 - 1990
N2 - 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.
AB - 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.
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UR - http://www.scopus.com/inward/citedby.url?scp=84907035128&partnerID=8YFLogxK
U2 - 10.3109/10601339009024025
DO - 10.3109/10601339009024025
M3 - Article
AN - SCOPUS:84907035128
VL - 8
SP - 99
EP - 112
JO - Clinical Research Practices and Drug Regulatory Affairs
JF - Clinical Research Practices and Drug Regulatory Affairs
SN - 1060-1333
IS - 2
ER -