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
- IRB chairs' perspectives on genotype-driven research recruitment.. 34:1-10. 2012
- Women's views about participating in research while pregnant.. 34:1-8. 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
- Developing model language for disclosing financial interests to potential clinical research participants.. 29:1-5. 2007
- Who should go first in trials with scarce agents? The views of potential participants.. 29:1-6. 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