Ernest D Prentice

Biographic Data

ID7169245
NAMEErnest D Prentice
GIVEN NAMESErnest D
FAMILY NAMEPrentice
SIGNATUREPRENTICE E D
AFFILIATIONSInstitute of Economic Affairs
VERIFIEDNo
TOTAL WORKS12
TOTAL CITATIONS0
WORKS AS AUTHOR12
WORKS AS EDITOR0
FIRST PUBLICATION YEAR1989
LATEST PUBLICATION YEAR2003
H-INDEX0

  • Women in Early Phase Trials

    James R Anderson, Toby Schonfeld et al.ARTICLEIRB Ethics and Human Research2003

    James R. Anderson, Toby L. Schonfeld, Timothy K. Kelso, Ernest D. Prentice, Women in Early Phase Trials: An IRB's Deliberations, IRB: Ethics & Human Research, Vol. 25, No. 4 (Jul. - Aug., 2003), pp. 7-11

  • Conflict between Research Design and Minimization of Risks in Pediatric Research

    Bruce Gordon, Bruce G Gordon et al.ARTICLEIRB Ethics and Human Research2000

    Bruce Gordon, Ernest Prentice, James Anderson, Conflict between Research Design and Minimization of Risks in Pediatric Research, IRB: Ethics & Human Research, Vol. 22, No. 3 (May - Jun., 2000), pp. 1-6

  • Selective Review of External Adverse Events

    Bruce Gordon, Bruce R Gordon et al.ARTICLEIRB Ethics and Human Research1999

    Bruce Gordon, Ernest Prentice, Selective Review of External Adverse Events: One IRB's Response to the Avalanche of IND Safety Reports, IRB: Ethics & Human Research, Vol. 21, No. 3 (May - Jun., 1999), pp. 10-11

  • IRB Review of Adverse Events in Investigational Drug Studies

    Ernest D Prentice, Bruce Gordon et al.ARTICLEIRB Ethics and Human Research1997

  • Continuing Review of Research Involving Human Subjects

    Bruce Gordon, Ernest D Prentice et al.ARTICLEIRB Ethics and Human Research1997

    Bruce Gordon, Ernest Prentice, Continuing Review of Research Involving Human Subjects: Approach to the Problem and Remaining Areas of Concern, IRB: Ethics & Human Research, Vol. 19, No. 2 (Mar. - Apr., 1997), pp. 8-11

  • Ethical Considerations in Informed Consent for Potential Future Use of Human Tissue Samples

    Mary Adams, Mary L Adams et al.ARTICLEIRB Ethics and Human Research1996

    Mary Adams, Ernest D. Prentice, Gwenn S. F. Oki, Ethical Considerations in Informed Consent for Potential Future Use of Human Tissue Samples, IRB: Ethics & Human Research, Vol. 18, No. 2 (Mar. - Apr., 1996), pp. 6-7

  • The Use of Normal Children as Participants in Research on Therapy

    Bruce Gordon, B A Gordon et al.ARTICLEIRB Ethics and Human Research1996

  • The Case of Two Devices

    James R Anderson, Andrew Jameton et al.ARTICLEIRB Ethics and Human Research1995

    James R. Anderson, Andrew Jameton, Paul J. Reitemeier, Ernest Prentice, The Case of Two Devices: Disclosure to Subjects Following Phase IV ("Post-Marketing") Research, IRB: Ethics & Human Research, Vol. 17, No. 3 (May - Jun., 1995), pp. 6-9

  • An Update on the PEG-SOD Study Involving Incompetent Subjects

    Ernest D Prentice, L Antonson et al.ARTICLEIRB Ethics and Human Research1994

    Ernest D. Prentice, L. Antonson, Lyal G. Leibrock, Vikram C. Prabhu, Timothy K. Kelso, Thomas D. Sears, An Update on the PEG-SOD Study Involving Incompetent Subjects: FDA Permits an Exception to Informed Consent Requirements, IRB: Ethics & Human Research, Vol. 16, No. 1/2 (Jan. - Apr., 1994), pp. 16-18

  • Bill of Rights for Research Subjects

    Ernest D Prentice, Paul J Reitemeier et al.ARTICLEIRB Ethics and Human Research1993

  • Consistency in Interpreting Federal Regulations Helps Assure Equitable Treatment of Subjects

    Ernest D PrenticeARTICLEIRB Ethics and Human Research1993

  • Can Children Be Enrolled in a Placebo-Controlled Randomized Clinical Trial of Synthetic Growth Hormone

    Ernest D Prentice, L Antonson et al.ARTICLEIRB Ethics and Human Research1989

    Ernest D. Prentice, L. Antonson, Andrew Jameton, Benjamin Graber, Thomas Sears, Can Children Be Enrolled in a Placebo-Controlled Randomized Clinical Trial of Synthetic Growth Hormone?, IRB: Ethics & Human Research, Vol. 11, No. 1 (Jan. - Feb., 1989), pp. 6-10