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Study Coordinator ChecklistPI:Sponsor:Protocol #:Study Title:Number of Anticipated Study Subjects:Steps Check (?) When CompletedComments 1Send the following to CHLAclinicalresearch@chla.usc.edu:1.
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Gather all necessary information and documentation such as names and contact information of involved parties, details of the agreement, terms and conditions, and any supporting documents or references.
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Who needs contracts and clinical researchchildrens?

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Contracts and clinical research involving children refer to agreements and studies focused on children's health, medical treatments, and interventions, ensuring ethical standards and regulatory compliance.
Researchers, institutions, and organizations conducting clinical trials or studies involving children are typically required to file contracts related to such research.
To fill out contracts and clinical research involving children, one should provide accurate study details, participant information, ethical considerations, and gain necessary approvals from relevant authorities.
The purpose of these contracts is to establish legal agreements for conducting research, protect the rights of child participants, ensure their safety, and ensure compliance with regulations.
Information that must be reported includes study objectives, participant demographics, consent processes, study protocols, and any potential risks or benefits to child participants.
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