GMPc Vietnam JSC
  • About Us  
    • Summary information
    • Key Personnel
  • Services  
    • WHO GMP Pharmaceutical facilities  
      • Project feasibility study
      • Technology and Equipment consultation
      • Detail Construction and MEP drawing
      • Project Management and Supervision
      • WHO GMP Training and Guidance
      • Preparation of WHO GMP registration dossier
      • WHO GMP Re-evaluation consultation
    • EU GMP Pharmaceutical Factory  
      • Feasibility study report
      • Design detailed construction drawings
      • QM documentation – Validation
      • GMP application and product dossier application
      • Project management - Construction supervision
    • CGMP, ISO 22716-certified cosmetics facilities  
      • Project feasibility study
      • Technology and Equipment consultation
      • Detail Construction and MEP drawing
      • Project Management and Supervision
      • CGMP ASEAN Training and Guidance
      • Preparation of CGMP ASEAN/ ISO 22716 registration dossier
      • CGMP ASEAN Re-evaluation consultation
    • Health-supplement facilities  
      • Project feasibility study
      • Technology and Equipment consultation
      • Detail Construction and MEP drawing
      • Project Management and Supervision
      • HS GMP Training and Guidance
      • Preparation HS GMP registration dossier
      • HS GMP - Re-evaluation consultation
    • Eligibility For Cosmetic Manufacturing  
      • Overall consultation
      • Detail Construction and MEP drawing
      • Designing, Constructing, Ensured Certification
      • Preparation of Registration Dossier
    • Pharmaceutical distribution center  
      • Feasibility Study
      • Design and Information Technology Solutions
      • Project Management and Supervision
      • GSP registration and operation consultancy
    • GSP warehouses  
      • Project feasibility study
      • Detail Construction and MEP drawing
      • GSP Training and Guidance
      • Overall Consultation on Designing And Constructing
      • GSP Re-evaluation consultation
    • Veterinary Pharmaceutical Facilities  
      • Project Feasibility Study
      • Technology and Equipment consultation
      • Detail Construction and MEP Drawing
      • Project management and Supervision
      • WHO GMP Training and Guidance
      • Preparation of WHO GMP registration dossier
      • WHO GMP Re-evaluation consultation
    • GMP, GLP, GSP training  
      • Basis knowledge
      • Intensive Training
    • Other GPs’s consultation  
      • GLP inspection laboratories
      • GDP distribution systems
      • GPP pharmacy
      • WHO GACP medicinal materials
    • Register and Announce  
      • Announcement of Imported Cosmetic
    • Dairy Factory  
      • Overall Planning
      • Detailed Construction & MEP Design - Project Budgeting
      • Contractor/Supplier Consultation and Project Management
      • Training, Drafting registration dossier
  • Project
  • Video
  • GMP-Handbook
  • Faqs
  • News
  • Jobs
  • Contact

    SERVICES

  1. Home
  2. SERVICES
  3. PHARMACEUTICAL DISTRIBUTION CENTER

List of services

  • Pharmaceutical Facilities
  • EU GMP Pharmaceutical Factory
  • Health Supplement Facilities
  • CGMP, ISO 22716-certified Cosmetics Facilities
  • Eligibility for cosmetic manufacturing
  • GSP Warehouses
  • Pharmaceutical Distribution Center
  • Dairy Factory
  • GMP, GLP, GSP Training
  • Other GPs’s consultation

Typical projects

Nippon Chemiphar Pharmaceutical Facility - GMP certification

Nippon Chemiphar Pharmaceutical Facility - GMP certification

Hapharco Pharmaceutical Warehouse - GSP certification

Hapharco Pharmaceutical Warehouse - GSP certification

Hau Giang Pharmaceutical Facility - WHO GMP certification

Hau Giang Pharmaceutical Facility - WHO GMP certification

VIMAC Cosmetic Facility - CGMP ASEAN Certification

VIMAC Cosmetic Facility - CGMP ASEAN Certification

Pharmaceutical distribution center

30/06/2021 | 3082

Pharmaceutical distribution center

The strategy of Pharmaceutical Industry and Government

"The national development strategy for phamarceutical industry to 2020, vision to 2030" clearly indicates: 05 pharmaceutical distribution centers will be built in the Northern mountainous areas, the North Central, the South Central Coast-Central Highlands, the Southeast and Southwest region;

Decision No.376/QD-TTg dated March 17, 2021 on "Approving development program for the pharmaceuticals industry and domestically produced herbal until 2030 and vision to 2045" added: Investment on building and rearrangement of the distribution system, wholesale, retail, and domestical pharmaceutical transportation to be modern, professional and efficient. Encouraging application of EU-GSDP technical standards, building pharmaceutical storage warehouses and transport vehicles system with high technical standards.

The differences between Pharmaceutical Distribution Center and General Pharmaceutical Warehouse?

The Pharmaceutical Distribution Center is a modern, advanced model, that integrating the general warehouse following GSP regulations with a full range of Logistics services: Order processing, Shipping management, Supervision management, Testing/Packaging service,...

 

Pharmaceutical distribution center 02

 

The value of Pharmaceutical Distribution Center

1. Customers (pharmaceutical distributors)

Financial benefits

  • No need to invest in GSP warehouses, GDP facilities, means of transport, etc.
  • No need to pay operating and maintenance costs
  • Only pay rental cost that depends on the actual amount of goods for storage (m3/day or pallets/day)
  • Minimize the number/cost of specialized and operating personnel 

Convenience

  • Do not waste time for building facilities, personnel systems, and processes, ..
  • Professional and responsible partner
  • Full range of Logistics service: Order processing, delivery, reporting, ...

Quality of service is guaranteed

  • Guaranteed quality (Storage conditions - Online monitoring, Periodic reports)
  • Professional packaging
  • Meet the schedule, on-time delivery

Compliance with the Adminstrative Department requirements

  • No need/Minimize reporting
  • Conditions in compliance with requirements

2. Government Administration

  • Convenient for centralized Quality Management
  • Easily collect statistical data for forecasting and building strategy

3. Society

  • Improve the drug quality
  • Contribute to lower drug prices by reducing intermediate distributors.

4. Project Investor

  • The pioneering, modern and sustainable service model
  • Satisfied all of customers' expectations, even more than that.
  • Bring high economic efficiency

5. Enterprise/Support services

  • Development of transportation services that require temperature control and special storage
  • Development of the production and service realted to Packaging, packaging materials, labeling, ..

 

GMPc Vietnam

Related services

Project Management and Supervision

Project Management and Supervision

GSP registration and operation consultancy

GSP registration and operation consultancy

Design and Information Technology Solutions

Design and Information Technology Solutions

Feasibility Study

Feasibility Study

Typical partner

  • GMPc Vietnam JSC
  • Head Office: No. 18, Mang Cam 1 Street, An Lac Green Symphony, Van Canh Ward, Hoai Duc District, Hanoi City
  • Business location : No. 32, Vi Cam 5 Street, An Lac Green Symphony, Van Canh Ward, Hoai Duc District, Hanoi City
  • Tel: 0243.787.2242 | CEO hotline: 0982.866.668
  • Email: contact@gmp.com.vn
  • Representative Office: 156/1/1, Cong Hoa Street - Ward 12 - Tan Binh District - Ho Chi Minh City
  • Tel: 0283.811.7383 
  • Quick link
  • About Us
  • Services
  • Project
  • GMP-Handbook
  • Video
  • Consulting for cosmetic facility
  • Consulting for health supplement facility
  • Consulting for GSP warehouse
  • Fanpage
Facebook

Copyright © 2020 GMPc. All rights reserved.

  • Home
  • About Us
    • Summary information
    • Key Personnel
  • Services
    • WHO GMP Pharmaceutical facilities
      • Project feasibility study
      • Technology and Equipment consultation
      • Detail Construction and MEP drawing
      • Project Management and Supervision
      • WHO GMP Training and Guidance
      • Preparation of WHO GMP registration dossier
      • WHO GMP Re-evaluation consultation
    • EU GMP Pharmaceutical Factory
      • Feasibility study report
      • Design detailed construction drawings
      • QM documentation – Validation
      • GMP application and product dossier application
      • Project management - Construction supervision
    • CGMP, ISO 22716-certified cosmetics facilities
      • Project feasibility study
      • Technology and Equipment consultation
      • Detail Construction and MEP drawing
      • Project Management and Supervision
      • CGMP ASEAN Training and Guidance
      • Preparation of CGMP ASEAN/ ISO 22716 registration dossier
      • CGMP ASEAN Re-evaluation consultation
    • Health-supplement facilities
      • Project feasibility study
      • Technology and Equipment consultation
      • Detail Construction and MEP drawing
      • Project Management and Supervision
      • HS GMP Training and Guidance
      • Preparation HS GMP registration dossier
      • HS GMP - Re-evaluation consultation
    • Eligibility For Cosmetic Manufacturing
      • Overall consultation
      • Detail Construction and MEP drawing
      • Designing, Constructing, Ensured Certification
      • Preparation of Registration Dossier
    • Pharmaceutical distribution center
      • Feasibility Study
      • Design and Information Technology Solutions
      • Project Management and Supervision
      • GSP registration and operation consultancy
    • GSP warehouses
      • Project feasibility study
      • Detail Construction and MEP drawing
      • GSP Training and Guidance
      • Overall Consultation on Designing And Constructing
      • GSP Re-evaluation consultation
    • Veterinary Pharmaceutical Facilities
      • Project Feasibility Study
      • Technology and Equipment consultation
      • Detail Construction and MEP Drawing
      • Project management and Supervision
      • WHO GMP Training and Guidance
      • Preparation of WHO GMP registration dossier
      • WHO GMP Re-evaluation consultation
    • GMP, GLP, GSP training
      • Basis knowledge
      • Intensive Training
    • Other GPs’s consultation
      • GLP inspection laboratories
      • GDP distribution systems
      • GPP pharmacy
      • WHO GACP medicinal materials
    • Register and Announce
      • Announcement of Imported Cosmetic
    • Dairy Factory
      • Overall Planning
      • Detailed Construction & MEP Design - Project Budgeting
      • Contractor/Supplier Consultation and Project Management
      • Training, Drafting registration dossier
  • Project
  • Video
  • GMP-Handbook
  • Faqs
  • News
  • Jobs
  • Contact
 
Hotline: 0982.866.668
Nhắn tin Facebook Zalo: 0982.866.668