Drug Clinical Trials Management

Some of the comprehensive clinical trial management services we offer to our clients are as follows:

• Research Protocol Design

• Sample Size Calculation

• Case Report Form Design

• Informed Consent Form Design

• Ethics Committee and TİTCK Application File Preparation

• Center Feasibility and Selection

• Monitoring Management

• Project Management
• Study Materials Inventory
• Researcher Meeting Planning and Coordination
• Center Organization Management
• Data Management and Data Entry Support Service
• Statistical Analysis and Reporting
• Medical Writing Services
• Import and Customs Procedures
• Adverse Event/Serious Adverse Event Monitoring and Reporting
• Center Specific File Management
• Regulatory File Management
• Training Services
• Laboratory Contract Negotiations
• Revolving Fund Contract Processes
• IT and Technical Consulting

With our expert team in the field, we provide meticulous service at every stage of clinical trials and ensure the successful progress of your projects.