IRB review of adverse events in investigational drug studies

Ernest D. Prentice, Bruce Geoffrey Gordon

Research output: Contribution to journalReview article

6 Citations (Scopus)
Original languageEnglish (US)
Pages (from-to)1-4
Number of pages4
JournalIRB Ethics and Human Research
Volume19
Issue number6
StatePublished - Nov 1 1997

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research personnel
Human Experimentation
Ethical Review
Government Regulation
Mandatory Reporting
Investigational Drugs
Research Subjects
Consent Forms
Ethics Committees
Federal Government
Research Ethics Committees
cost-benefit analysis
United States Food and Drug Administration
Drug-Related Side Effects and Adverse Reactions
Informed Consent
Ethics
risk assessment
Cost-Benefit Analysis
moral philosophy
Research Personnel

ASJC Scopus subject areas

  • Social Sciences(all)

Cite this

IRB review of adverse events in investigational drug studies. / Prentice, Ernest D.; Gordon, Bruce Geoffrey.

In: IRB Ethics and Human Research, Vol. 19, No. 6, 01.11.1997, p. 1-4.

Research output: Contribution to journalReview article

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