CRF Name:
Adverse Events
Description:
The Adverse Events (AEs) CRF Module documents medical events that occur to a participant/subject once enrolled in a study. The AE form includes: the AE start date, severity, relatedness, outcome, and an indication of whether the event is serious.
Copyright:
False
CRF Type:
CRF Module
CRF Extension:
.doc
CRF Search Data:
CRF Upload User:
mbeyers@emmes.com
CRF Upload Date:
2013-01-10 12:02:40.497
CRF Order Old:
100
Version Number:
4.10
Version Date:
2012-06-29 00:00:00.0
CRF Coming Soon:
0
CDE Coming Soon:
0
Form Note:
External Link Text:
CRF
Checklist:
0
Annotation Extension:
Annotation Search Data:
Annotation Upload User:
Annotation Upload Date:
Old CRF Module URL:
Doc/General/Safety Data/Adverse Events/Adverse_Event_CRF_Module.doc
Old Annotation Url:
Short Name:
Adverse_Events
Rights Claims:
44
External Url:
Doc/SharedForms/F0009_Adverse_Events.docx