PRG Flashcards
ACRP
Association of Clinical Research Professional
AE
Adverse Event
CCRT
Certified Clinical Research Training
CCRT
Core Clinical Research Training
CLIA
Clinical Laboratory Improvement Amendments
COI
Conflict of Interest
CRA
Clinical Research Associate
CRO
Clinical Research Organizer
CTA
Clinical Trials Assistant
CTMS
Clinical Trials Management System
CV
Curriculum Vitae
DHHS (HHS)
Dep’t of Health and Human Services
DMC
Data Monitoring Committee
DMP
Data Monitoring Plan
DOA Log
Delegation of Authority
DSMB
Data Safety Monitoring Board
DUA
Data User Agreement
ECRF
Electronic Case Report Form
EDC
Electronic Date Cap(?)
EMR
Electronic Medical Record
ePRO
electronic Patient Reported Outcome
FDA
Federal Drug Administration
HIPAA
Health Insurance Portability and Accountability Act
HUD
Housing and Urban Development
IB
Investigator’s Brochure
IBC
Institutional Biosafety Committee
ICF
Informed Consent Form
IDE
Investigational Drug Exemption
IDS
Investigational Drug Services
IND
Investigational New Drug/Device
IP
Investigational Product
ISF
Investigator Site File
ISPCTN
Idea States Pediatric Clinical Trials Network
LAR
Legally Authorized Representative
MOP
Manual of Procedures
MOO
Manual of Operations
MRN
Medical Record Number
NTF
Note to FIle
OCR
Office of Clinical Research
OHRP
Office For Human Resarch Protections
ORSP
Office of Research and Sponsored Programs
PA
Program Assistant
PC1/2
Program Coordinator
PCTG
Pediatric Clinical Trial Group
PHI
Personal Health Info
PHN
Pediatric Hearth Network
PI
Principal Investigator
PM
Program Manager
PM
Project Manager
PRA
Prospective Reimbursement Analysis
PRG
Pediatric Research Group
PTN
Pediatric Trials Network
RA
Research Assistant
SAPRC
Services Pricing Application for Research Centers
SCTR
South Carolina Clinical And Translational Research Institute
SOP
Standards of Procedures
WIRB
Western Institutional Review Board