Acronyms
A B C D E F G H I J K L M N O P Q R S T U V W X Y Z
AE
|
Adverse Event
|
AI
|
Avian Influenza
|
BFS
|
Batch Flow Sheet
|
CRF
|
Case Report Form
|
CTSS
|
Clinical Trial Support Specialist
|
DCS
|
Data Collection Site
|
DM
|
Data Management
|
DSMB
|
Data Safety Monitoring Board
|
EC
|
Ethics Committee
|
FHI
|
Family Health International
|
FWA
|
Federal Wide Assurance
|
GCP
|
Good Clinical Practice
|
GLP
|
Good Laboratory Practice
|
GPP
|
Good Pharmacy Practice
|
IC
|
Informed Consent
|
ICH
|
International Conference on Harmonization
|
IND
|
Investigational New Drug
|
IRB
|
Institutional Review Board
|
MOP
|
Manual of Operations
|
MOU
|
Memorandum of Understanding
|
NIAID
|
National Institute of Allergy and Infectious Disease
|
NIH
|
National Institutes of Health
|
NCC
|
Network Coordinating Center
|
NSC
|
Network Steering Committee
|
OHRP
|
Office of Human Research Protections
|
OUCRU
|
Oxford University Clinical Research Unit
|
PI
|
Principal Investigator
|
PVF
|
Protocol Violation Form
|
QA
|
Quality Assurance
|
QC
|
Quality Control
|
RCHSPB
|
Regulatory Compliance and Human Subjects Protection Branch
|
SAE
|
Serious Adverse Event
|
SAIC
|
Science Applications International Cooperation
|
SEAICRN
|
South East Asia Infectious Disease Clinical Research Network
|
SC
|
Study Coordinator
|
SMC
|
Site Management Committee
|
SOP
|
Standard Operating Procedure
|
TOC
|
Trial Operations Committee
|