Medical Affairs Solutions

Medical Affairs Consulting and Human Resource Solutions

CMIC Group provides comprehensive solutions related to medical affairs, including Medical Affairs consulting, contract Medical Science Liaisons, medical information service, and clinical research support services for evidence building. In order to meet the growing demand for medical affairs support, we provide customized solutions that match individual companies’ needs. Our solutions are based on our experience and knowledge of the Japanese market, with customized, optimum solutions.

Medical Affairs Solutions at CMIC

Medical Affairs Solutions
- MA Consulting
- Operational Support
- Human Resources Solutions
- MA/MSL Training
Medical Information Call Center
Clinical Research
- Project management
- Clinical monitoring
- Data management
- Clinical research administration office support (Certified review board/ethics committee submission, clinical research contract, document storage and management, site payment, etc.)
- Medical writing
- Pharmacovigilance
- Data Monitoring Committee (DMC) support

*The link will direct you to website of CMIC Inizio Co., Ltd.

Our Edge in Medical Affairs

Medical Professionals’ Communication Skills

With accumulated know-how in communicating successfully with more than 50 clients, we educate our staff to develop skills and increase our performance as Medical Affairs professionals.
As medical information service, our call center has highly experienced communicators with experience as pharmacists and nurses. Healthcare professionals can receive answers about appropriate use of pharmaceutical drugs, OTC drugs, cosmetics and health foods/functional foods.

Extensive Experience

Each of our consultants employ professional expertise in an array of areas, offering high-quality consulting services.

Strong Regulatory Authority Knowledge

Experience with a wide range of regulatory matters and various authorities including PMDA and MHLW, including preparation of supporting data, application dossiers and responses to the authorities’ queries.

Contribution to the creation of evidence that builds the pharmaceutical life cycle

Comprehensive support for various types of clinical research, such as interventional study, observational study, clinical trial in accordance with “Clinical Trials Act”, multinational clinical research in accordance with ICH-GCP, etc.