Acronyms Flashcards by Liz Trieu

Q

ADR

A

Adverse Drug Reaction

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Q

AE

A

Adverse Event

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Q

BID

A

Twice a day

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Q

BMI

A

Body Mass Index

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Q

BP

A

Blood Pressure

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Q

C

A

Celsisus

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Q

CAPA

A

Corrective and Preventive Action

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Q

CRA

A

Clinical Research Associate (study monitor)

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Q

CRC

A

Clinical Research Coordinator

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Q

CRF

A

Case Report Form

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Q

CRO

A

Contract Research Organization

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Q

CTMS

A

Clinical Trial Management System

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Q

CV

A

Curriculum Vitae

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Q

eCRF

A

Electronic Case Report Form

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Q

ePRO

A

Electronic Patient Reported Outcomes

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Q

EDC

A

Electronic Data Capture

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Q

EMR

A

Electronic Medical Record

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Q

F

A

Fahrenheit

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Q

GCP

A

Good Clinical Practice

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Q

GLP

A

Good Laboratory Practices

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Q

GMP

Study These Flashcards

A

Good Manufacturing Practices

Q

hCG

Study These Flashcards

A

Human Chorionic Gonadotropin

Q

IB

Study These Flashcards

A

Investigator’s Brochure

Q

ICF

Study These Flashcards

A

Informed Consent Form

ICH

International Conference on Harmonization

IP

Investigational Product

IRB

Institutional Review Board

IEC

Independent Ethics Committee

IVRS

Interactive Voice Response System

IWRS

Interactive Web Response System

LAR

Legally Acceptable Representative

Mcg

Microgram

mmHg

Millimeters of mercury

NSAID(s)

Non-Steroidal Anti-Inflammatory Drug(s)

PI

Principal Investigator

PK

Pharmacokinetics

PRO

Patient Reported Outcomes

p.r.n

as needed

QA

Quality Assurance

QC

Quality Control

QD or OD

Once a Day

QID

Four Times a Day

RBM

Risk Based Monitoring

SAE

Serious Adverse Event

SMO

Site Management Organization

SOP

Standard Operating Procedure

SUSAR

Suspected Unexpected Serious Adverse Reaction

TMF

Trial Master File

OSDI

Ocular Surface Disease Index

FDF

Financial Disclosure Form