Indexed keywords
ARTICLE;
CLINICAL ETHICS;
ETHICS;
HUMAN;
INFORMED CONSENT;
INTERPERSONAL COMMUNICATION;
PATIENT SELECTION;
PROSPECTIVE STUDY;
RESEARCH;
RESEARCH ETHICS;
STANDARD;
CLINICAL ETHICS;
INFORMED CONSENT;
RESEARCH ETHICS;
ETHICS, RESEARCH;
HUMANS;
INFORMED CONSENT;
PATIENT SELECTION;
PROSPECTIVE STUDIES;
RESEARCH;
TRUTH DISCLOSURE;
1
84895011469
accessed Jan 2013
http://clinicaltrials.gov/ct2/show/NCT00513747 (accessed Jan 2013).
2
67650001781
The obligation to participate in biomedical research
Schaefer G, Emanuel E, Wertheimer A. The obligation to participate in biomedical research. JAMA 2009;302:67-72.
(2009)
JAMA , vol.302
, pp. 67-72
Schaefer, G.1
Emanuel, E.2
Wertheimer, A.3
3
0037921904
The Nuremberg Code
Nuremberg Code. (accessed Jan 2013)
Nuremberg Code. The Nuremberg Code. 1949. http://ori.dhhs.gov/education/products/RCRintro/c03/b1c3.html (accessed Jan 2013).
(1949)
4
84894939970
111 Criteria for IRB approval of research
Common Rule 45 CFR.
Common Rule 45 CFR.111 Criteria for IRB approval of research.
5
84894925489
accessed Jan2013
http://www.ciscrp.org/patient/infocenter/BillofRights.pdf (accessed Jan2013).
6
84864004729
Terminating clinical trials without sufficient subjects
Damen L, van Agt F, de Boo T, et al. Terminating clinical trials without sufficient subjects. J Med Ethics 2012;38:413e-6.
(2012)
J Med Ethics , vol.38
Damen, L.1
Van Agt, F.2
De Boo, T.3
7
79954517832
The successful integration of research and care: how pediatric oncology became the subspecialty in which research defines the standard of care
Unguru Y. The successful integration of research and care: how pediatric oncology became the subspecialty in which research defines the standard of care. Pediatr Blood Cancer 2011;56:1019-25.
(2011)
Pediatr Blood Cancer , vol.56
, pp. 1019-1025
Unguru, Y.1
8
78049311495
Lack of study volunteers hobbles cancer fight
New York Times, August 2
Kolata G. Lack of study volunteers hobbles cancer fight. New York Times, August 2, 2009.
(2009)
Kolata, G.1
9
0003991809
Patient recruitment in clinical trials
Raven Press, New York
Spilker B, Cramer JA. Patient recruitment in clinical trials. Raven Press, New York, 1992.
(1992)
Spilker, B.1
Cramer, J.A.2
10
84864004729
Terminating clinical trials without sufficient subjects
Damen L, van Agt F, de Boo T, et al. Terminating clinical trials without sufficient subjects. J Med Ethics 2012;38:413e-6, 415.
(2012)
J Med Ethics , vol.38
Damen, L.1
Van Agt, F.2
De Boo, T.3
11
84864004729
Terminating clinical trials without sufficient subjects
Damen L, van Agt F, de Boo T, et al. Terminating clinical trials without sufficient subjects. J Med Ethics 2012;38:413e-6, 416.
(2012)
J Med Ethics , vol.38
Damen, L.1
van Agt, F.2
de Boo, T.3
12
84894985473
Guidelines for Good Clinical Practice
International Conference on Harmonisation of Technical Requirements for Registration of Pharmaceuticals for Human Use
International Conference on Harmonisation of Technical Requirements for Registration of Pharmaceuticals for Human Use. Guidelines for Good Clinical Practice, 1997.
(1997)
13
0009625051
Making informed consent meaningful
Brody B. Making informed consent meaningful. IRB 2001;23:1-5.
(2001)
IRB , vol.23
, pp. 1-5
Brody, B.1
14
0003663231
Principles of biomedical ethics
5th edn. New York: Oxford University Press
Beauchamp T, Childress C. Principles of biomedical ethics. 5th edn. New York: Oxford University Press, 2011:65.
(2011)
, vol.65
Beauchamp, T.1
Childress, C.2
