Risk to bystanders in clinical trials: A symposium

Research output: Contribution to journalArticle

Abstract

This symposium takes a critical look at the ethics of impact on “bystanders” to clinical research. By that we mean study non-participants who nevertheless are at risk of being affected by the study in some way. This introduction suggests some questions to consider while reading through the symposium contributions, and gives a précis of each.

Original languageEnglish (US)
Pages (from-to)447-449
Number of pages3
JournalClinical Trials
Volume16
Issue number5
DOIs
StatePublished - Oct 1 2019

All Science Journal Classification (ASJC) codes

  • Pharmacology

Keywords

  • bystander
  • Clinical trials
  • human research subject protection
  • informed consent
  • research ethics
  • research non-participant
  • research subject
  • third-party consent

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