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. WHO GMP

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

Project management and Supervision

27/01/2022 | 672

Project management  and Supervision

Project Management and Supervision 
“Ensuring project quality, progress, cost, and construction safety followed construction design combining with the drafting of IQ, OQ, PQ documents.”

In general, the facility construction project, which comply with WHO GMP requirements, are composed of many aspects, each of them has high specialization such as:

  • Construction: Easily cleaning, ensuring the prevention or limitation of contaminations, cross-contaminations and outside intrusions. 
  • HVAC Systems: Require the stability of temperature, humidity, pressure, controlled input airflow, Cleanliness.
  • RO/ Distilled water/ Wastewater treatment System: Compliance with GMP requirements, pharmacopoeia and specific requirements of each type of products.

Therefore, taking the responsibility of project management, supervision and equipment installation requires the consultant to have extensive knowledge and more important to clearly understand the purpose of Use, the auxiliary equipments, the GMP-facility requirements, ... Only competant consultant can ensure project quality, cost, progress, construction safety and resolve many other problems occur during implementation.

With GMPc service, we will help you to managing and supervising the project construction. Moreover, GMPc will proactively draft and complete the documentation system (IQ,OQ,PQ,SOP,..) during the installation of equipment, in order to finalize GMP-evaluation process right after construction completes.

" GMPc is a project management consultant for facility construction project in compliance with WHO GMP requirements. Our services are professional, effective and guaranteed for equipment installation with corresponding IQ,OQ,PQ,SOP documents."

GMP c  Vietnam

Related services

Project Feasibility Study

Project Feasibility Study

Technology and Equipment consultation

Technology and Equipment consultation

Detail Construction and MEP Drawing

Detail Construction and MEP Drawing

WHO GMP Training and Guidance

WHO GMP Training and Guidance

Preparation of WHO GMP registration dossier

Preparation of WHO GMP registration dossier

WHO GMP Re-evaluation consultation

WHO GMP Re-evaluation consultation

Typical partner

  • GMPc Vietnam JSC
  • Head Office: Blue Office, 4- BT1, Bui Xuan Phai Street, My Dinh 2 Ward, Nam Tu Liem 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 - Fax: 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