Other CCRP Flashcards

1
Q

Institutional Review Board (Ethics Committee)

A

IRB

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2
Q

National Cancer Institute
National Institutes of Health

A

NCI

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3
Q

Food and Drug Administration

A

FDA

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4
Q

Office of Human Research Protections

A

HHS

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5
Q

Adverse Event

A

AE

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6
Q

Serious Adverse Event

A

SAE

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7
Q

Adverse Drug Reaction

A

ADR

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8
Q

Contract Research Organization

A

CRO

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9
Q

Site Management Organization

A

SMO

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10
Q

Good Clinical Practice

A

GCP

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11
Q

Clinical Research Associate

A

CRA

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12
Q

Case Report Form

A

CRF

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13
Q

Principle Investigator

A

PI

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14
Q

International Conference on Harmonisation of Technical Requirements for Registration of Pharmaceuticals for Human Use

A

ICH

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15
Q

Code of Federal Regulations

A

CFR

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16
Q

Investigational New Drug

A

IND

17
Q

National Institutes of Health Health and Human Services

A

NIH

18
Q

Standard Operating Procedure

A

SOP