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COVER PAGE: OFFICIAL TITLE: Phase II Study of (RAD001,) for Children with Recurrent or Progressive Ependymoma NCT number: NCT02155920 Document date: June 7, 2020Page 1 of 18Version 7/31/17DO NOT Disclosed
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crad001cus224t consent eng 20170731docx is a consent form used for regulatory or compliance purposes, typically related to customer consent for specific actions or processes.
Individuals or organizations that are handling customer data or seeking consent for specific actions related to data processing are required to file this document.
To fill out crad001cus224t consent eng 20170731docx, one must provide required information such as customer details, specific consent statements, and any relevant dates. Ensure all fields are accurately completed and signed as needed.
The purpose of this document is to obtain and record customer consent for processing their data, ensuring compliance with applicable data protection laws.
The information that must be reported includes customer identification details, the scope of consent, the purpose for data processing, and any relevant contact information of the responsible party.
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