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