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describes how to abstract and edit the administrative details of clinical trials.

About Administrative Data

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About Administrative Data - Include v4.4
About Administrative Data - Include v4.4

Abstracting General Trial Details

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Abstracting General Trial Details - Include v4.4
Abstracting General Trial Details - Include v4.4

Abstracting Collaborators

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Abstracting Collaborators - Include v4.4
Abstracting Collaborators - Include v4.4

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Abstracting Human Subject Safety

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Abstracting Human Subject Safety - Include v4.4
Abstracting Human Subject Safety - Include v4.4

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Abstracting INDs and IDEs

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Abstracting INDs and IDEs - Include v4.4
Abstracting INDs and IDEs - Include v4.4

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Abstracting NCI-Specific Information

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Abstracting NCI-Specific Information - Include v4.4
Abstracting NCI-Specific Information - Include v4.4

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Abstracting Participating Sites

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Abstracting Participating Sites - Include v4.4

Abstracting Regulatory Information

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Abstracting Regulatory Information - Include v4.4

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Abstracting Trial Statuses

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Abstracting Trial Statuses - Include v4.4
Abstracting Trial Statuses - Include v4.4

Abstracting Funding

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Abstracting Funding - Include v4.4
Abstracting Funding - Include v4.4

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Abstracting Trial-Related Documents

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Abstracting Trial-Related Documents - Include v4.4
Abstracting Trial-Related Documents - Include v4.4

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