- 3/4/19 - 1 form, 13 itemgroups, 47 items, 1 language
Itemgroups: Administrative documentation, Serious Adverse Event, Serious Adverse Event, Seriousness of Adverse Event, Serious Adverse Event, Demographics Domain, Serious Adverse Event, Experimental Drug, Serious Adverse Event, Causations, Disease, Serious Adverse Event, Risk Factors, Serious Adverse Event, Concomitant Agent, Investigational New Drugs, Serious Adverse Event, Evaluation, Serious Adverse Event, Comment, Confirmation, Clinical Investigators