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.

Our Edge in Consulting

CMIC Group Strategic and Regulatory Consulting for Pharmaceutical companies

Resources

  • C-CAST: In-Country Clinical Caretaker (ICCC) for Clinical Trials in Japan

Oncology Drug Development
  • Unlocking Japan: Navigating Clinical Trials and Market Potential for Global Biopharma

Oncology Drug Development

Have inquiries about our services or are you interested in outsourcing your operations to us?

Commercial

Comprehensive Sales and Marketing Support
Human Resources Solutions for MR
Remote Communication Support
Training/Assessment

Medical Affairs

MA Consulting
Operational Support
Human Resources Solutions for MA/MSL
MA/MSL Training

Patient Solutions

Patient Support Programs
Nurse Educator