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Table 3 Description of reporting targets of adverse events by sponsors

From: Assessing the detection, reporting and investigation of adverse events in clinical trial protocols implemented in Cameroon: a documentary review of clinical trial protocols

 

National sponsors

International sponsors

Target to report adverse events

  

Expected adverse events

 Investigator

1

5

 Sponsor

1

13

 DSMB

0

1

 Ethics Board

1

4

 Not specified

28

43

 Total

31

71

Unexpected adverse events

 Investigator

0

2

 Sponsor

0

7

 DSMB

0

1

 Ethics Board

1

3

 Others

1

10

 Not specified

29

50

 Total

31

71