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Registering or amending Complete trials in the CTRP involves organizations and persons that have the following roles in clinical trials: lead organization, sponsor, principal investigator, and so on. CTRP does not manage information about persons and organizations; instead, this is delegated to the Person and Organization Curation Portal, also known as PO. For more information, refer to the NCI CTRP Person and Organization Curation Portal User 's Guide.

Note
You must have a user account with appropriate LDAP membership to access the PO User's Guide.

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