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Page History
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This page tree describes how to abstract and edit the administrative details of clinical trials.
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Abstracting General Trial Details
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Abstracting Collaborators
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Abstracting Human Subject Safety
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Abstracting INDs and IDEs
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Abstracting NCI-Specific Information
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Abstracting Participating Sites
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Abstracting Regulatory Information
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Abstracting Trial Statuses
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Abstracting Funding
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Abstracting Trial-Related Documents
Include Page
