CRC Acronyms Flashcards

(46 cards)

1
Q

ADME

A

Absorption, Distribution, Metabolized, Excretion

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
2
Q

ADR/AE

A

Adverse drug reaction/asverse event

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
3
Q

CDA

A

Confidentiality disclosure agreement

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
4
Q

CDM

A

Clinical Data Management

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
5
Q

CRF

A

Code of Federal Regulations

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
6
Q

CNS

A

Central nervous system

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
7
Q

CRA

A

Clinical research associate

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
8
Q

CRO

A

Contract Research Organization

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
9
Q

CRF

A

Case report form

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
10
Q

CRS

A

Clinical regulatory specialis

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
11
Q

DEa

A

Drug enforcement admin

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
12
Q

EC

A

Ethics Commitee

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
13
Q

GCP

A

Good clinical practice

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
14
Q

GLP

A

Good laboratory practice

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
15
Q

HREC

A

Human research ethics committees

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
16
Q

HMO

A

Health management organizations

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
17
Q

IB

A

Investigator Brochure

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
18
Q

IC/F

A

Informed Consent/F

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
19
Q

ICH

A

International conference of harmonisation

20
Q

IEC

A

Independent Ethics Committee

21
Q

IRB

A

Institutional Review Board

22
Q

IRDB

A

Investigator research database

23
Q

ISFN

A

Investigator site file notebook

24
Q

LOI

A

Letter of intent

25
LREC
Local research ethics committee
26
MAP
Master action plan
27
MREC
Multi Research Ethinc Committee (UK)
28
NDA
New drug application
29
PI
Principal Investigator
30
PIS
Patient information sheet
31
PM
Project manager
32
PQRS
PPD Query Resolution System
33
QA
Quality Assurance
34
QC
Quality control
35
RA
Research Assistant
36
RCM
Research coordinator manager
37
RCR
Regulatory Compliance Review
38
RTMS
Research Trial Management System
39
SAE
Serious Adverse Event
40
SC
Study Coordinator
41
SMF
Study master file
42
SMO
Site Management Organization
43
SOP
Standard Operating Procedures
44
TAL
Training Attendance log
45
TMF
Trial Master File
46
WHO
World Health Organization