- > 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
Accurate and speedy writing greatly influence the speed of application and licensing.
Providing assurance and reliability based on proven successes and performance.
- Scientific Advisor
- To incorporate advice and proposals from professionals, CMIC has established the Scientific Advisor. CMIC reflects professional opinions in every operation.
- Extensive experience and know-how as a CRO
- As a pioneering CRO, CMIC uses its experience and know-how accumulated over years in each project.
- Accumulation of knowledge and information
- CMIC can always access the latest knowledge and information due to its acceptance of wide-ranging business requests from various customers.
- Preparation of investigator's brochures (draft)
- Protocol development (draft) and documentation
- Preparation of informed consent and supplementary materials for subjects
- Preparation of case report forms (drafts)
- Preparation of clinical study reports (drafts)
- Support for adverse event reports
- Support for application summary preparation
- SOP preparation
- Support for publication
- Support for preparation of orphan drug designation application
- SGML
- CTD
