Was established in

2013

Through 10 years

Co-Branding

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.

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

ACHIEVEMENTS
TOGASHI TSUNEHIRO

CM Plus Group Founder and Chairman

MESSAGE OF THE CM PLUS GROUP FOUNDER AND CHAIRMAN

Hello Everyone,
I came to Vietnam and started working for CMPV since 2013 and then live in Ho Chi Minh City since 2014 after I sold out my house in Japan. That fact proves how much I would like to get closely involved myself in Vietnam country. Working with foreigners is my dream, especially bringing up to the local specialists who are engineers some good expertise and making them understand about GMP and Validation works for Pharmaceutical and Medical device industries. Our team/ Our company CMPV is still small but all members’ capability is so high and they are still developing it throughout the actual projects. I feel very happy when some of clients appreciate my staff’s work and behaviour which they try to contribute for clients always. CMPV has been contributing and will contribute the level up of GMP for Vietnamese pharmaceutical and medical device companies. Please come visit our homepage to see what we are doing. Thank you very much with our best regards.

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TAHARA SHIGEHIRO

CM Plus Vietnam’s Chairman

MESSAGE OF THE CM PLUS GROUP FOUNDER AND CHAIRMAN

Hello Everyone,
I came to Vietnam and started working for CMPV since 2013 and then live in Ho Chi Minh City since 2014 after I sold out my house in Japan. That fact proves how much I would like to get closely involved myself in Vietnam country. Working with foreigners is my dream, especially bringing up to the local specialists who are engineers some good expertise and making them understand about GMP and Validation works for Pharmaceutical and Medical device industries. Our team/ Our company CMPV is still small but all members’ capability is so high and they are still developing it throughout the actual projects. I feel very happy when some of clients appreciate my staff’s work and behaviour which they try to contribute for clients always. CMPV has been contributing and will contribute the level up of GMP for Vietnamese pharmaceutical and medical device companies. Please come visit our homepage to see what we are doing. Thank you very much with our best regards.

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SERVICES

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.

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.

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.

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.

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 vi *GMP: Good Manufacturing Practice *GDP: Good Distribution Pra

OUR PARTNERS