AdverseEventReporting / Study — Study
Active
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FHIR: 0 resource(s),
0 attribute(s) mapped
Qualified: AdverseEventReporting::Study
If the adverse reaction or event occured while the patient was participating in a study (e.g., a clinical trial), this class will contain identifying information about that study.
Attributes / الخصائص
| Code | Name | Type | FHIR | Req |
|---|
No attributes yet.
FHIR Mapping (MOH → FHIR) / مواءمة FHIR
No FHIR resource mapping for this class.
Mappings (MOH → Models) / المواءمات
No benchmark mappings for this class.
Consumer Mappings / مواءمة المستفيدين
No consumer mappings for this class.