According to Keiko Oishi, president and COO of CMIC, “The global health care industry is going through a significant change. The types of service request and qualification requirements are changing, the number of global trials is increasing, and study designs are more complex.”
A CMIC spokesperson told us that the company will provide feedback regarding Japanese CRO’s circumstances for developing technology standards. They added, “CMIC will join forces with global CRO partners to continue to develop open technology standards that makes it easier for sponsors and CROs to run collaborative clinical trials.”
The CRO specializes in using IT technology to create new methods for clinical trials and uses real-world data to create cost-efficient models. CMIC has worked as a solutions provider for clinical operations and implemented the use of virtual trials in the area.
CMIC provides end-to-end solutions from preclinical to clinical trials, drug development, and manufacturing, and from filing to post-market surveillance.