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Keyword Analysis & Research: brazil medical device reporting
Keyword Analysis
Keyword
CPC
PCC
Volume
Score
Length of keyword
brazil medical device reporting
0.39
0.8
1374
7
31
brazil
0.8
0.9
1886
16
6
medical
0.34
0.4
7331
31
7
device
0.94
0.1
5733
23
6
reporting
1.93
1
1244
29
9
Keyword Research: People who searched brazil medical device reporting also searched
Keyword
CPC
PCC
Volume
Score
brazil medical device adverse event reporting
0.66
1
3602
46
medical device regulation brazil
1.19
1
2914
100
brazil medical device regulations
0.34
0.9
4031
80
brazil medical device database
1.87
0.4
421
41
brazil medical device standards
0.98
0.3
4092
78
medical device registration brazil
1.05
0.1
7860
43
brazil medical device classification
1.47
1
6221
66
brazil medical device classification rules
1.19
1
7196
68
brazil medical device registration fee
1.23
1
6459
82
brazil anvisa medical device regulations
2
0.4
8394
83
fda medical device reporting database
1.4
0.1
2989
84
medical device reporting for manufacturers
0.04
0.1
8685
57
electronic medical device reporting
1.98
0.6
7355
72
medical device reporting guidance
0.92
0.8
1746
91
medical device reporting fda
1.94
0.9
8741
45
medical device reporting fda guidance
0.34
0.5
1202
38
latin america medical devices report
0.48
0.9
3909
65
medical device adverse event reporting
1.87
0.8
3451
14
fda medical device adverse event reporting
1.71
0.3
8256
64
china medical device adverse event reporting
1.71
0.1
2966
33
japan medical device adverse event reporting
1.45
0.8
7355
72
medical device adverse event reporting form
0.28
0.3
1873
45
medical device adverse event database
0.82
0.4
5080
88
fda adverse event medical device
0.94
0.9
8315
39
medical device adverse event
0.37
0.2
2444
100
adverse event reporting system fda
1.52
0.5
8320
1
fda adverse event reporting database
1.11
0.3
6340
100
medwatch adverse event reporting
0.39
0.3
3105
5
fda's medwatch adverse event reporting
0.57
0.1
8888
2
fda guidance for adverse event reporting
1.55
0.4
8380
98
adverse event reporting fda
1.11
0.4
7207
40
fda guidance on reporting adverse events
0.35
0.6
3433
93
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