Acronym ADR AE APEX CA CAP CCRP CFR CHR CITI COI CRA CRC CRF CRO CRRM CRS CTA CTCAE CTSI DA DM DSMB DSMC DSMP DUA ECRF EDC EMR FDA FWA GCP HIPAA HRPP IB ICF ICD ICH IDE IND IRB iRIS ITA ITR Name Adverse Drug Reaction Adverse Event Epic based electronic medical records at UCSF Coverage Analysis Corrective Action Plan Certified Clinical Research Professional Code of Federal Regulations Committee on Human Research (former name for UCSF IRB) Collaborative IRB Training Initiative Conflict of Interest Clinical Research Associate Clinical Research Coordinator Case Report Form Contract Research Organization Clinical Research Risk Manager Clinical Research Services Clinical Trials Agreement Common Terminology Criteria for Adverse Events Clinical and Translational Science Institute Division Administrator Department Manager Data Safety Monitoring Board Data and Safety Monitoring Committee Data and Safety Monitoring Plan Data Use Agreement Electronic Case Report Form Electronic Data Capture Electronic Medical Record Food and Drug Administration Federal wide Assurance Good Clinical Practice Health Insurance Portability and Accountability Act Human Research Protection Program Investigator’s Brochure Informed Consent Form Industry Contracts Division International Conference on Harmonization Investigational Device Exemption Investigational New Drug Institutional Review Board Online IRB application system at UCSF Office of Innovation, Technology and Alliances Investigational Trial Resource (Cancer Center) acronymn list 26feb18 MCA MOP MRN MTA NIH NTF OCR OHRP OSR PHI PI PRN QA QC QIU RFA RMIS RMS RN RSC SAE SEV SFVAMC SIV SOC SOE SOP Sub-I Medicare Coverage Analysis Manual of Procedures Medical Record Number Material Transfer Agreement National Institutes of Health Note to File Office of Clinical Research Office for Human Research Protection Office of Sponsored Research Protected Health Information Principal Investigator As Needed Quality Assurance Quality Control Quality Improvement Unit Research Financial Analyst Risk Management and Insurance Services Research Management Services Registered Nurse Research Services Coordinator Serious Adverse Event Site Evaluation Visit Veterans Administration Medical Center Site Initiation Visit Standard of Care Schedule of Events Standard Operating Procedure Sub-Investigator acronymn list 26feb18
