CRC Protocols and Standard Operating Procedures
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C-01-01
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Completion of Case Report Forms (CRFs)
CRC Application - Acknowledgement of Publication
CRC Application - Budget Submission and Approval
CRC Application - Initial CRC Application
CRC Application - Protocol Approval for CRC Utilization
CRC Application - SAC Executive Protocol Review
CRC Application - SAC Review Ranking Process
CRC Protocol Document System - Add Edit or Delete Users
CRC Protocol Documents System - Initial Document Upload
Obtaining and Documenting Informed Consent
Operation and Performance - Bionutrition Services
Operation and Performance - CRC Electronic Order Sets
Operation and Performance - CRC Orders
Operation and Performance - CRC Study Initiation
Operation and Performance - Establishing Subject Eligibility.pdf
Operation and Performance - Freezer Maintenance Protocol
Operation and Performance - Site Training for Institutional Staff
Operation and Performance - Stable Isotope Compounding
Principal Investigator Monitoring of Study Conduct
Principal Investigator Responsibilities
Regulatory - Investigational Agent Management
Regulatory - IRB Approval and Maintenance
Regulatory - Subject Confidentiality
Translation of Consent Forms
Unanticipated Problem and Serious Adverse Event (SAE) Reporting
Unit Administration - CRC Research Charts
Unit Administration - Initial Visit Checklist
Unit Administration - Preparing, Approving, Distributing CRC SOPs
Unit Administration - Scheduling for CRC Protocols
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