Exam 6 Flashcards

1
Q

A technology that enables you to convert different types of documents into editable and searchable data is

A

OCR

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2
Q

After a subject is off-study, newly identified adverse events or serious adverse events can be reported for ____days the end of protocol treatments

A

30 days

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3
Q

A congenital anomaly/bird defect is an example of _____adverse events or suspected adverse reaction

A

Serious

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4
Q

AERS is ?

A

Adverse Event Reporting System

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5
Q

Managing the coordinating center is an essential function of ??

A

Leas Site staff

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6
Q

Any noxious changes which is suspected to be due to a drug, occurs at doses normally used, required treatment or decrease in dose or indicates caution in the future use of the same drug is ???

A

Adverse Drug Reaction

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7
Q

For the reportable SAE, the protocol is a timeline within _____from the time the investigator was notified of the event.

A

24 hr

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8
Q

If the AE continues and the subject is off the study, check the _____box

A

Continuing AE

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9
Q

DTMF is ?

A

Dual Tone Multi Frequency signaling

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10
Q

The subject number changes with the subsequent phase of the study

A

False

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11
Q

Events that meet the definition of Unanticipated problems must be submitted within ____business days of becoming aware of the event

A

2days

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12
Q

A statistical tool within VIGI search that allows filtering of the results by demographic

A

IGIMINE

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13
Q

When responsiveness diminishes rapidly after administration of a drug, the response is ?

A

Tachypylaxis

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14
Q

Risk assessment should be completed ____the protocol

A

Before

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15
Q

Protection of human subject is 21CFR ___?

A

50

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16
Q

21 CRF 56 deals with

A

IRB

17
Q

______cover large populations with detailed information on exposed and unexpected patients.

A

Longitudinal Electronic Patients Record

18
Q

Appearance of toxic effects in a recipient to therapeutic doses of drugs is called ?

A

Intolerance

19
Q

Electronic CRF should not be preferred over paper CRF

True or False

A

False

20
Q

______contains information regarding all AEs reported in all trials of the test article.

A

Investigational Brochure

21
Q

The report of events to the FDA is done in the form of ??

A

IND Safety Report

22
Q

_____is restricted to small fraction of population

A

Cohort Event Monitoring

23
Q

NOAEL is ?

A

No observed effect level

24
Q

Inspections done on issues concerning drug safety are :

A

Targeted Inspections

25
Q

The assessment of efficacy of response of drug to the dose is done in ??

A

Phase 2b