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- Part I - Informed Consent for Research: Operationalizing the Process
- Part II - Informed Consent for Research: The Importance of Quality for Understanding and Decision-Making
- A Primer on Clinical Research
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- Bedside Nursing "Want to Write a Research Protocol?"
- Bedside Nursing "From Clinical Inquiry to Conducting Nursing Research"
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- OHRP’s Thinking on Key Revisions to the Common Rule
- Creating and Sustaining Diverse Study Enrollment: Towards a Quantifiable Science of Recruitment
- Applying the Principles of the Science of Safety to Improve Subject Safety in Clinical Research: Actionable Practices to Identify and Minimize Risk
- The Evolution of Vulnerability – The Ethics of Equitable Subject Selection
- The Reality of Enrollment Expectations
- Including Vulnerable Subjects with Cognitive Impairment in Research
- Minimally Disruptive Research: A Respectful Approach to Conducting Clinical Studies
- The Evaluation of Evidence for Regulatory Decision Making
- Recent Advances in the Early Detection of Alzheimer's Disease
- E-Consent: Usability Issues
- Informed Consent
- Affordable Care Act and Research: Where Have We Been and Where Are We Going
- An Update from the Patient-Centered Outcomes Research Institute (PCORI)
- Utilizing the Research Ehtics Review Process as a Method to Incorporate Quality by Design
- OHRP’s Thinking on Key Revisions to the Common Rule
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