Ethical Conduct of Clinical Research Involving Children (2004) / Chapter Skim
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References
References
Pages 277-308
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1996. Motivation for participation in clinical trials of drugs for the treatment of asthma, seasonal allergic rhinitis, and perennial nonallergic rhinitis.
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In: Amdur RJ. Institutional Review Board Member Handbook.
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national pediatric cancer clinical trials. Journal of Pediatric Hematology and Oncology 19(5)
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. Federal agency says oral history is not subject to rules on human research volunteers.
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2001. Breaking the camel's back: Multicenter clinical trials and local institutional review boards.
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2002. International Ethical Guidelines for Biomedical Research Involving Human Subjects.
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1998. Protection of human subjects: Categories of research that may be reviewed by the institutional review board (IRB)
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Federal Register 68:3541535416. Dickert N, Grady C
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1991a. Protection of human subjects; informed consent; standards for institutional review boards for clinical investigations.
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2003a. Draft financial relationships and interests in research involving human subjects: Guidance for human subject protection.
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1996. Scientific Research: Continued Vigilance Critical to Protecting Human Subjects.
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: A paradigm of a clinical trials network for genetic and orphan diseases. Advanced Drug Delivery Reviews 54(11)
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. Statement on behalf of the American Society of Transplantation, Children's Hospital Boston, and the North American Pediatric Renal Transplant Coop erative Study to the Committee on Clinical Research Involving Children.
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2000a. Choice of Control Group and Related Issues in Clinical Trials: E10.
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2000a. Protecting Data Privacy in Health Services Research: Committee on the Role of Institutional Review Boards in Health Services Research Data Privacy Protection.
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2000. Defining and describing benefit appropriately in clinical trials.
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2002. Media, public scrutinize clinical trials.
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1995. Research consent by adolescent minors and institutional review boards.
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2003. Perceptions of patients and physi cians regarding phase I cancer clinical trials: Implications for physician-patient commu nication.
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2002. How Have Pediatric Clinical Trials Influenced Practice: Past and Future.
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1999. Policy of the National Cancer Institute for Data and Safety Monitoring of Clinical Trials.
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1998a. NIH Policy and Guidelines on the Inclusion of Children as Participants in Research Involving Human Subjects, March 6, 1998.
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1998c. Institutional Review Boards: Their Role in Reviewing Approved Research.
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2001. The Globalization of Clinical Trials: A Growing Challenge in Protecting Human Subjects.
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Examples of Multicenter Phase I Clinical Trials Conducted Through the Cystic Fibrosis Therapeutics Development Network Between 2001 and 2003. Seattle, WA: Cystic Fibrosis Research Center, University of Washing ton.
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. Statement on Behalf of the Allergy & Asthma Network/Mothers of Asthmatics to the Committee on Clinical Research Involving Children.
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2004. How do institutional review boards apply the federal risk and benefit standards for pediatric research?
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2003. Groups potentially at risk for making poorly informed decisions about entry into clinical trials for childhood cancer.
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1998. Informed consent for clinical trials: Is simpler better?
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2003. Testimony before the Committee on Clinical Research Involving Children.
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In: National Bioethics Advisory Commission. Research Involving Human Biological Materials: Ethical Issues and Policy Guidance, Vol.
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2002. World Medical Association Declaration of Helsinki: Ethical Principles for Medi cal Research Involving Human Subjects.
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