- > Pre-clinical trials
- > Consultation for product development and planning
- > Monitoring
- > Data management
- > Medical writing
- > Patient access / recruitment
- > Site management / Study Coordinator
- > Pharmacovigilance
- > Audit
- > EDC solution
Extensive and abundant clinical trial experiences in Japan
CMIC can propose custom-tailored solutions based on information such as clinical trials in medical facilities and the expected number of cases in different fields.
- High-quality employee training
- A specialized educational division has been established at CMIC for improvement of staff quality.
- It provides introductory and continuing education and leadership development.
- Project management
- CMIC promises fast accomplishment of each contracted project by setting benchmarks for quantitative management.
- Japan's largest CRA resource
- CMIC has Japan's largest CRA resource, both contracted and temporary combined.
- Provision of information for investigative sites
- CMIC proposes the best solution based on the performance, clinical area and prospective sample size of participating investigative sites
- English-language monitoring capabilities
- Project coordinators are proficient in English, ensuring that the exchange of detailed case information is smooth and reliable.
- Quality control overseen by an independent division
- Quality control functions are performed by an independent division to ensure the reliability of all aspects of contract work, record-keeping, and results.
- Project management
- Global development
- Selection of investigative sites
- Effective and accurate selection of investigative sites based on performance and experience in monitoring and CRC
- Patient registration
- Monitoring
- Japan's largest number of CRAs (proper personnel allocation to meet the client's needs)
- Nationwide network
- Largest contract numbers and share
