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Ernest D. Prentice [12]Ernest Prentice [7]
  1. Institutional Review Board assessment of risks and benefits associated with research.Ernest D. Prentice & Bruce G. Gordon - forthcoming - National Bioethics Advisory Commission 6705 Rockledge Drive, Suite 700, Bethesda, Maryland 20892-7979 Telephone: 301-402-4242• Fax: 301-480-6900• Website: Www. Bioethics. Gov.
     
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  2.  19
    The Use of Normal Children as Participants in Research on Therapy.Bruce Gordon, Ernest Prentice & Paul Reitemeier - 1996 - IRB: Ethics & Human Research 18 (3):5.
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  3.  16
    Women in early phase trials: an IRB's deliberations.James R. Anderson, Toby L. Schonfeld, Timothy K. Kelso & Ernest D. Prentice - 2002 - IRB: Ethics & Human Research 25 (4):7-11.
  4.  20
    Can Children Be Enrolled in a Placebo-Controlled Randomized Clinical Trial of Synthetic Growth Hormone?Ernest D. Prentice, L. Antonson, Andrew Jameton, Benjamin Graber & Thomas Sears - 1989 - IRB: Ethics & Human Research 11 (1):6.
  5.  41
    Ethical considerations in informed consent for potential future use of human tissue samples.Mary Adams, Ernest D. Prentice & Gwenn S. F. Oki - 1995 - IRB: Ethics & Human Research 18 (2):6-7.
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  6.  46
    The Case of Two Devices: Disclosure to Subjects Following Phase IV ("Post-Marketing") Research.James R. Anderson, Andrew Jameton, Paul J. Reitemeier & Ernest Prentice - 1995 - IRB: Ethics & Human Research 17 (3):6.
  7.  9
    Conflict between research design and minimization of risks in pediatric research.Bruce Gordon, Ernest Prentice & James Anderson - 2000 - IRB: Ethics & Human Research 22 (3):1.
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  8.  32
    Continuing Review of Research Involving Human Subjects: Approach to the Problem and Remaining Areas of Concern.Bruce Gordon & Ernest Prentice - 1997 - IRB: Ethics & Human Research 19 (2):8.
  9.  15
    Selective review of external adverse events: one IRB's response to the avalanche of IND safety reports.Bruce Gordon & Ernest Prentice - 1998 - IRB: Ethics & Human Research 21 (3):10-11.
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  10. The NIH Inclusion Guidelines: Challenges for the Future.Bruce Gordon, Ernest Prentice, Paul Reitemeier, William C. Waggoner & Barbara B. Sherman - 1996 - IRB: Ethics & Human Research 18.
     
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  11.  8
    An even safer safety net.Ernest Prentice - 1997 - Hastings Center Report 27 (3):46-46.
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  12.  21
    An Institutional Policy on the Right to Benefit from the Commercialization of Human Biological Material.Ernest D. Prentice, John C. Wiltse, John G. Sharp & Dean L. Antonson - 1990 - Journal of Law, Medicine and Ethics 18 (1-2):162-167.
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  13.  14
    An Institutional Policy on the Right to Benefit from the Commercialization of Human Biological Material.Ernest D. Prentice, John C. Wiltse, John G. Sharp & Dean L. Antonson - 1990 - Journal of Law, Medicine and Ethics 18 (1-2):162-167.
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  14.  7
    A Protocol Review Guide to Reduce IRB Inconsistency.Ernest D. Prentice & L. Antonson - 1987 - IRB: Ethics & Human Research 9 (1):9.
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  15.  36
    An Update on the PEG-SOD Study Involving Incompetent Subjects: FDA Permits an Exception to Informed Consent Requirements.Ernest D. Prentice, L. Antonson, Lyal G. Leibrock, Vikram C. Prabhu, Timothy K. Kelso & Thomas D. Sears - 1994 - IRB: Ethics & Human Research 16 (1/2):16.
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  16.  11
    Bill of Rights for Research Subjects.Ernest D. Prentice, Paul J. Reitemeier, L. Antonson, Timothy K. Kelso & Andrew Jameton - 1993 - IRB: Ethics & Human Research 15 (2):7.
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  17.  5
    Consistency in Interpreting Federal Regulations Helps Assure Equitable Treatment of Subjects.Ernest D. Prentice - 1993 - IRB: Ethics & Human Research 15 (1):11.
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  18.  17
    IRB Review of Adverse Events in Investigational Drug Studies. [REVIEW]Ernest D. Prentice & Bruce Gordon - 1997 - IRB: Ethics & Human Research 19 (6):1.
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  19.  16
    IRB Review of a Phase II Randomized Clinical Trial Involving Incompetent Patients Suffering from Severe Closed Head Injury. [REVIEW]Ernest D. Prentice, L. Antonson, Lyal G. Leibrock, Timothy K. Kelso & Thomas D. Sears - 1993 - IRB: Ethics & Human Research 15 (5):1.
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