Site Managment

• Feasibility Assessments
• Facilitating Contract Negotiations
• Providing sites, managed by CRC
• Providing fully dedicated coordinators and other staff
• Provides all study specific documentation from the sites
• Training the research teams to conduct trials according to ICH-GCP principles
• Development of study-specific support documents
• Organization of patients’ visits
• Organizing and managing satellite sites and facilities
• Keeping the constant communication between trial CRO/Sponsors, Bio Medical Services and the study teams
• Solving any legal or administrative issues
• Technical support and quality control the Investigators’ activities
• Reporting of the SAEs, according to the requirements
• Payment vendor services
• Archiving Services