Contract Development and Manufacturing Services

Global End-to-End CDMO Solutions

Bridging the US, Japan and Asia with Contract Development & Manufacturing Solutions

As the largest and first CRO in Japan, CMIC Group also has drug development expertise with advanced manufacturing and packaging platforms to help accelerate your drug development timeline. Whether you are launching new drugs in the U.S. or considering new market entry for the Japanese market, we are your partner for global product development with the ability to seamlessly transfer technologies across borders for manufacturing. With our broad offerings, we can help you tie your development and commercialization needs in the West with the East.

View All of CMIC's CDMO Solutions

Formulation, Process & Analytical Development
Investigational Product Manufacturing
Packaging and Labeling
Release and Stability Testing
Technology Transfer
Commercial Supply

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Our Edge in Contract Development & Manufacturing

Formulation Development Expertise

With advanced technologies and extensive industry experience, we can help clients overcome formulation challenges and increase development efficiency.
CMIC has a dedicated Pharmaceutical Development Center (PDC) in Japan, as well as specialized dose form technology development teams in the U.S. and South Korea, to support our clients’ global market development.

End-to-End Solutions

Providing all aspects of drug development and manufacturing needs: preformulation study, formulation & process development, investigational product manufacturing, commercial supply and product life cycle management (PLCM).

Broad Dosage Form Capabilities

CMIC’s dosage forms development and manufacturing capabilities include: solid forms, such as tablets, capsules, powders and granules; semi-solid forms, such as gels ointments, creams, toothpaste, and suppositories; injectable products, such as vials and ampoules.

Global Network to Ensure Steady Supply

We have a global manufacturing network with diverse, highly reliable technologies and successful site inspections (FDA, EMEA, PMDA and TGA) track record to meet our clients’ needs.