• Delegated staffs for professional feasibility study in multiple sites
• Site and PI recommendation
• Consultation for site/investigator selection
• Database Survey
• PI interview
• Trustworthy feasibility report

• Provide/Organize training & education programs for site staff
• Establish and coordinate investigator team
• Establish infra-structure for trials in hospitals
• One-stop service for internal & external parties in a site
• One-stop service for multiple sites within the network

• Provide dedicated, full-time and experienced Clinical Research Coordinators on-site
• Assist in visits and meetings arrangement & FU
• Assist in accelerating the processof IRB if possible
• Set up central recruitment campaign for trials
• Assist in the preparation and conduct of monitoring, audit and inspection

Sites

• Investigators and Sites need assistance
• Well-established infra-structure & well-trained, dedicated staff are essential for quality trial conduct and performance
• Good performance bring income and reputation to sites

Sponsor

• Efficient and accurate feasibility response
• Efficient contract process for multiple sites
• Efficient pre-study preparation
• Efficient subject recruitment
• Good compliance and high quality of conduct
• High retention rate for trial subjects
• Efficient query resolution

Patients

• In good hands
• 24 hours, 7 days a week, professional care