Contracted Clinical Trial
CXMJ will provide reasonable and speedy one-stop service while maintaining Know-how, manpower and promotion related system necessary for clinical trials of pharmaceuticals and medical devices.
In addition, by the specialists of clinical trial, CXMJ will support with a wide range of tasks including planning,monitoring(including EDC), QC/QA, DM/statistical analysis, safety information management, medical writing, and regulatory affairs, etc.
CXMJ will be willing to respond to requests such as inside and outside manufacturers, medical institutions, or SMOs to Academia and Venture Companies.
Professional features of CX Medical Japan
- Collaboration with experienced monitors and young monitors with strong consciousness enables speedy, high quality and low cost clinical trial progress.
- CXMJ will promote a speedy and smart clinical trial by taking advantage of IT system such as EDC.
- CXMJ collaborates with partner companies, and will manage clinical trials on a one-stop basis with high expertise and reliability.
- CXMJ will maintain high quality in both DM/BIOS, QC(quality control), and QA(quality assurance) operations through cooperation with experts inside and outside the company, and proceed the operations at low cost.