- > 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
Using its accomplishment of 50 protocols for more than 100 clinical trials and its know-how, CMIC promises faster results in clinical trials.
CMIC's emphasis on optimization and streamlining has brought subject sizes 1.3 to 3.0 times larger than any other competitors.
- CMIC's staff, trained in healthcare services and ranging from PR agents, nurses and clinical laboratory technologists to MRs, provides total support for subject recruitment.
- Wide-ranging services only the experienced CRO can provide
- Optimized and streamlined strategies for subject recruitment: unification of advertisement and the telecommunication center has successfully led to sample sizes 1.3-3.0 times larger than those of competitors.
- High-quality telecommunications by well-experienced nurses and operators
- Consulting
- Calculation of cost-per-subject for subject recruitment and prediction of sample size based on the client's clinical trial outline
- Support for documentation required for budget development and monitor briefing
- Selection of area and sites for subject recruitment
- Advertisement
- Consultation on profiling, geographical characterization and advertising media for the client's target disease
Selection of the most effective media and advertisement design proposals
Preparation of reports, including advertisement planning, production, implementation and effectiveness - Telecommunication service
- Manuals and FAQs for operators
Screening of eligible subjects
Referral to clinical trial sites
Project planning and execution of long-term care for enrolled subjects
