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Do You Know Me?: The Subtle Distinction Between “Anonymous” and “De-identified” Data in Clinical Research

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Making Clinical Research Inclusive: Strategies to Include the LGBTQIA+ Community in Research Trials

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The IRB’s Perspective: Determining Optimal Compensation for Clinical Trial Participants

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Providing Research Participants with New Information: Is “Re-Consent” Always Necessary?

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Informed Consent and COVID-19: An IRB Perspective on Navigating the New Normal

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An Overview of the Recent SACHRP Recommendations Around Payments in Clinical Research

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Infectious Disease Challenge Studies: Ethical Issues in Causing Disease for Medical Knowledge

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Is this an Interventional Clinical Trial or Observational Study? How- and Why- it is Important to Write Protocols that Make This Distinction Clear

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Clinical Trial Recruitment Practices: The Evolution of Ethical Considerations

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Ethical and Biosafety Oversight of Gene Transfer Clinical Research: What Sponsors and CROs Need to Know

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