Standard Operating Procedures Approved SOP's 1.1 FDA Inspection 2.8 Research Specimens 2.5 Communication with Subjects **REVISED May 2023** 2.6 Epic and OnCore Participant Management Processes 2.7 Reporting Adverse Events/Unanticipated Problems 2.1 Obtaining Informed Consent 2.2 Pre-Screening for Human Subject Research 2.3 Determining Eligibility for Human Subject Research Studies 2.4 Preparation for a Subject Visit InfoEd Resources OnCore Resources Research Storage Right-Side Nav ClinicalTrials.Gov Greenphire Research Experts Funding Institutional ECRT PeopleSoft infoEd OnCore Cayuse Pure REDCap TriNetX EHS Assist BioRender