Oncology
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Series: The Future of Clinical Research Sites
Endpoint Adjudication: Best Approaches for Streamlining and Reducing Site Burden
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Ethics in Clinical Research
Should Parents Be Allowed to View their Child’s Survey Responses?
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Clinical Trial Safety
WCG IRB Central and Institutional Site Relationships
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New Applications, New Use Cases: The Expanding Need for Endpoint Adjudication
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Ethics in Clinical Research
Drafting a Research Plan for IRB Review and Research Conduct: Information That Must Be Included in a Clinical Trial Protocol
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Hybrid & Decentralized Trials
Complex Clinical Trial Protocol Designs: The Impact on Research Sites and the Role of a Central IRB
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Series: Ask the IRB & IBC Experts
Adults with Limited Capacity to Consent to Research
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Ethics in Clinical Research
What are the requirements for notifications of study closure at research sites?
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Live Survey Results – Part 4: Complex Clinical Trial Protocol Designs: The Effect on Research Sites and the Role Central IRBs Play in Ensuring Quality
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