• Centralised Site and Study Monitoring
• Study Start Up Management
• Clinician Onboarding and Credentialing Management
• Global Compounds, Study and Experiment Management
• Global Contracting Agreements RFPs and Tender Management
• Project and Workgroup Management
• Site Identification and Selection
• Product Registration and Submission Management (RIM)
• Regulatory Intelligence Database (RID)
• Labeling Process and Material Management
• Medical Devices National Registry
• Study Design and Execution Life-cycle (SDEL)
• PMO, PLM & Product Strategy Management
• Identification of Drug and Medicinal Products (IDMP)
• Change Control Management (including SOPs)
.svg){kind=small}
.svg){kind=small}