- > 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
CMIC promises acceleration of clinical trials by encouraging subject enrollment.
Secure and strong support at participating medical institutions that is based on experience
- Almost all staff members are experienced nurses.
- 65% of CMIC coordinators are experienced nurses familiar with medical services and excellent in communication.
- Staff with a rich clinical experience
- CMIC's study coordinators are constituted of specialists with the highest qualifications and experience in the SMO industry. Three-year medical experience is an absolute requirement when individuals are recruited as coordinators.
- High-quality education and training
- Both inside and outside specialists offer training and education of coordinators on a regular basis and from a variety of aspects.
- Enriched support system
- By retaining well-experienced staff as support members, CMIC effectively controls the quality of study coordinators and provides consistently high-quality operations and services.
- On-site support at clinical trial briefings
- Schedule management for subjects
- Handling of investigational products
- Provision of information on side effects
- Consultation center
