II.
Domain overview
Reference · livedomain:clinical-trials
Clinical Trials overview
Design, execution, and analysis of clinical research studies — protocol design, patient recruitment, data management (EDC), adverse event monitoring, and regulatory submissions. Governed by FDA/EMA/ICH-GCP.
Attributes
displayName
Clinical Trials
description
Design, execution, and analysis of clinical research studies — protocol
design, patient recruitment, data management (EDC), adverse event
monitoring, and regulatory submissions. Governed by FDA/EMA/ICH-GCP.
Outgoing edges
contains2
- specialization:biomedical-informatics·SpecializationBiomedical Informatics
- specialization:clinical-informatics·SpecializationClinical Informatics
Incoming edges
applies_to2
- skill-area:clinical-data-management·SkillAreaClinical Data Management
- role:clinical-data-scientist·RoleClinical Data Scientist
applies_to_domain1
- workflow:clinical-trial-protocol·WorkflowClinical Trial Protocol Design