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Ethics Insights
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Ask the Experts
Ask the Experts
Employees as Research Participants
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Videos
Understanding the FDA’s new proposed regulations on human subject research and their impact on your clinical trial plans
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Blog Posts
Assessing Potential Risks in the Consideration of IND Exemption Criteria
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Blog Posts
Defining “Minimal Risk” in Clinical Research
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Should Parents Be Allowed to View their Child’s Survey Responses?
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Whitepapers
Drafting a Research Plan for IRB Review and Research Conduct: Information that Must Be Included in a Clinical Trial Protocol
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Whitepapers
Do You Know Me?: The Subtle Distinction Between “Anonymous” and “De-identified” Data in Clinical Research
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Does research involving retrospective review of patient charts require IRB review?
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Case Studies