GMPc Vietnam JSC
  • About Us  
    • Summary information
    • Key Personnel
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    • WHO GMP Pharmaceutical facilities  
      • Project feasibility study
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      • Detail Construction and MEP drawing
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      • 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
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Các dự án sản xuất vắcxin trong nước được hưởng nhiều ưu đãi

21/10/2014 | 804 | Tin tức Tổng hợp

Thủ tướng Chính phủ vừa cho phép áp dụng một số cơ chế, chính sách riêng cho các dự án đầu tư sản xuất vắcxin trong nước.
Đây là chính sách nhằm duy trì và phát triển sản xuất vắcxin trong nước để chủ động đáp ứng nhu cầu sử dụng vắcxin phòng bệnh cho nhân dân và hướng tới xuất khẩu.

sản xuất vacxin trong nước
Dây chuyền sản xuất vawcsxin tại Nhà máy sản xuất vawnxcxin Polyvac (Bộ Y tế). (Ảnh: TTXVN)
 
Cụ thể, các dự án đầu tư sản xuất vắcxin trong nước được vay vốn tín dụng đầu tư từ Ngân hàng Phát triển Việt Nam để đầu tư nâng cấp và đầu tư mới một số dây chuyền sản xuất vắcxin với mục tiêu sản xuất vắcxin thay thế một phần vắcxin phải nhập khẩu, đáp ứng nhu cầu chăm sóc sức khỏe của nhân dân. Theo đó, Nhà nước hỗ trợ lãi suất vay.

Các dự án đầu tư sản xuất vắcxin trong nước được áp dụng cơ chế chính sách quy định tại công văn số 918/TTg-KGVX ngày 8/6/2011 của Thủ tướng Chính phủ về cơ chế chính sách hỗ trợ dự án đầu tư sản xuất nguyên liệu kháng sinh.

Các dự án này cũng được giao, thuê 10 đến 15ha đất trong Khu công nghệ cao Hòa Lạc để xây dựng nhà máy sản xuất vắcxin, trước mắt ưu tiên cho đơn vị sản xuất vắcxin hiện đang có khó khăn về đất.


Thủ tướng Chính phủ giao Bộ Y tế xây dựng Đề án cụ thể theo quy định, trình Thủ tướng Chính phủ.

Theo thông tin từ Bộ Y tế, đến nay, Việt Nam là một trong số những nước đã tự sản xuất được khá nhiều loại vắcxin, trong số này có 10/12 loại vắcxin được sử dụng trong Chương trình tiêm chủng mở rộng, góp phần chủ động trong việc phòng chống dịch bệnh và đảm bảo an ninh sức khỏe cho nhân dân./.
Theo Vietnam+
 

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  • 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
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  • 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
 
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