Strategic and Regulatory Consulting
Comprehensive Consulting Services
Support Across All Clinical Trial Phases
CMIC Group provides consulting services that support drug development, Japanese/foreign market entry, clinical site network services, medical devices, regenerative medicine and Regulatory Affairs tasks. Our consultants are experts in product life cycle management, medical writing, med concierge services, drug development, regenerative medicine, in vitro diagnostics, medical devices and regulatory affairs. Our professional consultants bring their expertise to individual tasks, or as expert support for a clinical trial that CMIC is running for a customer. Click on the links below to discover how we can help streamline your project with on-demand services.