|
AE
|
Adverse Event
/ Adverse Experience
|
|
AR
|
Administrative Regulation ( UK )
|
|
CFR
|
Code of Federal Regulations
|
|
COI
|
Conflict of Interest
|
|
CR
|
Continuation Review
|
|
CRF
|
Case Report Form
|
|
CRO
|
Clinical Research Office ( UK )
|
|
CV
|
Curriculum Vitae
|
|
DHHS (or HHS)
|
Department of Health and
Human Services
|
|
DSMB
|
Data and Safety Monitoring
Board
|
|
DSMP
|
Data and Safety Monitoring
Plan
|
|
FDA
|
Food and Drug Administration
|
|
FR
|
Final Review
|
|
FWA
|
Federal Wide Assurance
|
|
GCP
|
Good Clinical Practice
|
|
GCRC
|
General Clinical Research
Center ( UK )
|
|
GIS
|
General Information Sheet
|
|
HHS (or DHHS)
|
Department of Health and Human Services
|
|
HIPAA
|
Health Insurance Portability
and Accountability Act (Privacy Rule)
|
|
IBC
|
Institutional Biosafety
Committee ( UK )
|
|
ICH
|
International Conference on
Harmonisation
|
|
IDS
|
Investigational Drug Service
( UK )
|
|
IRB
|
Institutional Review Board
|
|
JCAHO
|
Joint Commission on
Accreditation of Healthcare Organizations
|
|
KP
|
Key Personnel
|
|
LAR
|
Legally Authorized
Representative
|
|
NA (or N/A)
|
Not Applicable
|
|
NCI
|
National Cancer Institute
|
|
NIH
|
National Institute of Health
|
|
OHRP
|
Office for Human Research Protections
|
|
ORI
|
Office of Research Integrity
( UK )
|
|
OSPA
|
Office of Sponsored Projects
Administration ( UK )
|
|
PHI
|
Protected Health Information
|
|
PI
|
Principal Investigator
|
|
QIP
|
Quality Improvement Program
|
|
RDRC
|
Radioactive Drug Research Committee
|
|
RSC
|
Radiation Safety Committee ( UK )
|
|
SD
|
Source Document
|
|
SOP
|
Standard Operating Procedure
|
|
SP
|
Study Personnel
|
|
UK
|
University of Kentucky
|
|
UP
|
Unanticipated Problem
|
|
VA
|
Veterans Affairs
|
