Irb

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  Publication Venue For

  • Reducing Consent Form Length: Stakeholder Support, Evidence-Based Strategies, and Regulatory Requirements..  39:18-20. 2017
  • Barriers to Change in the Informed Consent Process: A Systematic Literature Review..  38:1-10. 2016
  • Certificates of confidentiality and informed consent: perspectives of IRB chairs and institutional legal counsel..  36:1-8. 2014
  • Women's views about participating in research while pregnant..  34:1-8. 2012
  • IRB chairs' perspectives on genotype-driven research recruitment..  34:1-10. 2012
  • An intervention to improve cancer patients' understanding of early-phase clinical trials..  31:1-10. 2009
  • Community hospital oversight of clinical investigators' financial relationships..  31:7-13. 2009
  • Who should go first in trials with scarce agents? The views of potential participants..  29:1-6. 2007
  • Developing model language for disclosing financial interests to potential clinical research participants..  29:1-5. 2007
  • Consent forms and the therapeutic misconception: the example of gene transfer research..  27:1-8. 2005
  • Can underpowered clinical trials be justified?.  26:16-19. 2004
  • Confidentiality: more than a linkage file and a locked drawer..  26:13-17. 2004
  • Children in research: new perspectives and practices for informed consent..  Suppl 25:S20-S23. 2003
  • Conducting empirical research on informed consent: challenges and questions..  Suppl 25:S4-S10. 2003