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 ”

ACHIEVEMENTS
<iframe src=”https://www.youtube.com/embed/Vjxgh034WyA” width=”560″ height=”315″ frameborder=”0″ allowfullscreen=”allowfullscreen”></iframe>SIK DAK FOOK RESTAUTANT
Togashi Tsunehiro

CM Plus Group Founder and Chairman

Message of the CM Plus Group Founder and Chairman

  • 世界的に視野に立ち常に最新の技術を駆使して顧客の繁栄に貢献しそこに働く私達が夢と生き甲斐を感じるそんな会社を目指す。
  • We seek to be a company with a global vision, always adopting the latest innovations to help our clients prosper, and giving ourselves a sense of aspiration and fulfillment.
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What we do

Pharmaceutical

. GMP consulting: we deliver professional services to provide best valued solutions to any questions that clients may have in relation to all international GMP standards such as EU-GMP (PIC/S), cGMP, J-GMP and WHO-GMP.

Medical devices

CM Plus is a professional consultant for medical device industry. We provide GMP consulting services to industries that must comply with PIC/S GMP, EU-GMP, cGMP or QSR (US FDA) and WHO-GMP for medical devices…

Food and Cosmetic

While regulatory compliance requirements are not as stringent as those in the Pharmaceutical and Medical Device industries, the Food and Cosmetic Industry has its own requirements for compliance to ensure product quality, in accordance with the regulations and guidance

Other industries

Beside pharmaceutical and medical device projects, we can also provide customers with Consulting, Engineering, Project and Construction Management, Bidding Consultancy services for Clean process projects, and projects with cleanrooms.

Services

1. Energy Conservation (Carbon Neutrality)

Manufacturing Companies in Southeast Asia Toward Carbon Neutrality

Direction in Southeast Asia Towards Carbon Neutrality: 
  • ASEAN’s Commitment*: “Carbon neutrality with 8 strategies” (i) accelerates green value chain integration, (ii) promote regional circular economy supply chains
  • EU Carbon Border Adjustment Mechanism (CBAM): Introduced in 2026
  • Supply Chain Shift to Southeast Asia: Geopolitical and economic impact
CM Plus’s Proposal:
  • Feasible Engineering Solution = Operation Optimization + Regulatory Knowledge
  • Keeping productivity with minimized environmental impact

2. 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

3. 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

4. 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

5. 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

6. 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

Our clients

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