Some of our comprehensive observational drug studies management services we offer to our customers;

•Research Protocol Design
• Sample Size Calculation
• Case Report Form Design
• Informed Consent Form Design
• Ethics Committee and TITCK application file preparation
• The Site Feasibility and Selection
• Monitoring Management
• Project Management
• Inventory Of Study Materials
• Planning and Coordination of Investigator Meeting
• Site Organization Management
• Data Management
• Data Entry Support Service
• Statistical Analysis and Reporting
• Medical Writing Procedures
• Import and customs procedures
• Adverse Events/Serious Adverse Events Monitoring and Collection
• Site Specific File Management
• Organizer File Management
• Training
• Laboratory Contract Negotiations
• Revolving Funds Agreements Negotiations
• BT and Technical Consulting