From Feasibility to Final Report
◆Trial Planning:
• Site identification & feasibility assessments
• Clinical development support in protocol designing
◆Trial Operations:
• Regulatory submissions & ethics approvals
• Trial monitoring & project management
• Vendor management
◆Data & Safety Oversight:
• Data management & biostatistics
• Medical monitoring
• Medical writing & safety reporting
◆Clinical Supplies & Logistics:
• Clinical trial supplies management
•Storage & warehousing for Investigational Product
• Re-packaging & labeling
