Was established in

2013

CM Plus Vietnam (CMPV) was established in 2013, head office in Ho Chi Minh City, is a subsidiary of CM Plus Group founded by Chairman Tsunehiro Togashi in 2007 in Yokohama, Japan.

Following the traditional services that our Group performs, CMPV develops services in the way that matches the Vietnam market and industries’ requirements. Our outstanding feature is to provide both critical services at the same time a Life Science project usually requests: Design solutions (from Concept to Details to implement) and GMP solutions to comply with GMP and other regulatory requirements that each industry may require in Vietnam and internationally.

Our business philosophy is to “bring new values” to clients. Those are closely related to the “beyond normal” success of a project by making full use of knowledge, capabilities and agility in applying innovative and evocative ideas in compliance with global standards.

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“A BEYOND NORMAL VALUE CREATOR
GOING ALONG WITH YOUR PROJECT ”

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Services

1. Consulting

For the purpose of ensuring quality at production facility of drugs/medical devices, we gather “knowledge” of first-rate consultants internationally and offers consulting services from the GMDP (GMP & GDP) / QMS / pharmaceutical regulatory affairs point of view *GMP: Good Manufacturing Practice *GDP: Good Distribution Practice *QMS: Quality Management System

2. Engineering

For the purpose of ensuring quality at production facility of drugs/medical devices, we gather “knowledge” of first-rate consultants internationally and offers consulting services from the GMDP (GMP & GDP) / QMS / pharmaceutical regulatory affairs point of vi *GMP: Good Manufacturing Practice *GDP: Good Distribution Practice *QMS: Quality Management System

3. Feasibility Study Report

For the purpose of ensuring quality at production facility of drugs/medical devices, we gather “knowledge” of first-rate consultants internationally and offers consulting services from the GMDP (GMP & GDP) / QMS / pharmaceutical regulatory affairs point of vi *GMP: Good Manufacturing Practice *GDP: Good Distribution Practice *QMS: Quality Management System

4. Project & Construction Management

For the purpose of ensuring quality at production facility of drugs/medical devices, we gather “knowledge” of first-rate consultants internationally and offers consulting services from the GMDP (GMP & GDP) / QMS / pharmaceutical regulatory affairs point of vi *GMP: Good Manufacturing Practice *GDP: Good Distribution Practice *QMS: Quality Management System

5. Bidding Support

For the purpose of ensuring quality at production facility of drugs/medical devices, we gather “knowledge” of first-rate consultants internationally and offers consulting services from the GMDP (GMP & GDP) / QMS / pharmaceutical regulatory affairs point of vi *GMP: Good Manufacturing Practice *GDP: Good Distribution Practice *QMS: Quality Management System

6. Other services

For the purpose of ensuring quality at production facility of drugs/medical devices, we gather “knowledge” of first-rate consultants internationally and offers consulting services from the GMDP (GMP & GDP) / QMS / pharmaceutical regulatory affairs point of vi *GMP: Good Manufacturing Practice *GDP: Good Distribution Practice *QMS: Quality Management System

Our activities