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Attachment 125STANDARD MONITORING DESK REVIEW Grantee ___Project No. ___Date of Review ___Type of Review ___Reviewer ___Grantee Staff Present ___1. GENERAL INFORMATION A. Grant/Loan Amount: ___ B.
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Chapter I - ctgov refers to the section of the Code of Federal Regulations that outlines the requirements for submitting clinical trial information to the ClinicalTrials.gov database.
Investigators and sponsors of clinical trials are required to file Chapter I - ctgov.
Chapter I - ctgov can be filled out online through the ClinicalTrials.gov website by providing all the required information about the clinical trial, including study design, interventions, and outcomes.
The purpose of Chapter I - ctgov is to provide transparency and public access to information about clinical trials, including their design, results, and participant eligibility criteria.
Information that must be reported on Chapter I - ctgov includes study design, participant eligibility criteria, interventions, outcomes, and adverse events.
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