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IRB Review of Adverse Events in Investigational Drug Studies

Bibliographic Data

ID13877599
AuthorsErnest D Prentice (corresponding author), Bruce Gordon (0000-0001-8760-9377), Bruce G Gordon
Year1997
Volume19
Issue6
Pages1-1
Publication date1997-11-01
Open AccessNo
TypeARTICLE
VenueIRB Ethics and Human Research (JOURNAL)
Journal identifiersISSN: 0193-7758 • E-ISSN: 2326-2222
PublisherHastings Center (PUBLISHER • US)
DOI10.2307/3564433
PMID11656910
OpenAlexW2473097146
LanguageEN
Citations received4

Adverse effect · Clinical trial · Drug · Intensive care medicine · Investigational Drugs · Medicine · Pharmacovigilance and Adverse Drug Reactions · Internal Medicine · Pharmacology

  • Mindsets, Informed Consent, and Research

    Open Access•Lynn A Jansen•The Hastings Center Report•2014

  • We Often Say We Lost Our Childhood, but I Think It Gave Us a Lot More than It Took Away’

    Open Access•Annamaria Neag, Victoria Nainova•Young•2025

  • "Research Ethics and the "Fieldwork Monitoring Committee

    Cristina Herrera, Chris Herrera•IRB Ethics and Human Research•2000

  • The IRB Is Not a Data and Safety Monitoring Board

    Elizabeth A Bankert, Elizabeth Bankert et al.•IRB Ethics and Human Research•2000

Citations per year0.15
Citation span2000 - 2025 (26)
Highly citedNo

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