Acronyms

 

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Network Policies and Guidelines

AE Adverse Event
AI Avian Influenza
BFS Batch Flow Sheet
CIRAS Center for International Research Assistance and Support
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 Federalwide 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
NRCC Network Regional 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
RDMC Regional Data Management Center
SAE Serious Adverse Event
SAIC Science Applications International Cooperation
SEA ICRN Southeast Asia Influenza Clinical Research Network
SMC Site Management Committee
SOP Standard Operating Procedure
TOC Trial Operations Committee



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