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Whitepapers Insights

Viewing all entries for: Whitepapers

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Women collaborating in an office, looking at charts on a tablet. Whitepapers

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

Read More about 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

Read More about 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

Read More about 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?

Read More about 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

Read More about 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

Read More about 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

Read More about 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

Read More about 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

Read More about 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

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