GMPc Vietnam JSC
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Nghiên cứu thành công vaccine cúm chỉ bằng 1/3 giá thuốc nhập khẩu

26/09/2018 | 1128 | Tin tức Tổng hợp

Ngày 25-9, tại TP Nha Trang, Khánh Hòa, Viện Vaccine và Sinh phẩm y tế (IVAC), Tổ chức Y tế thế giới (WHO) và một số tổ chức y tế khác phối hợp công bố kết quả dự án nâng cao năng lực phát triển vaccine cúm tại Việt Nam.
 
Nghiên cứu thành công vaccine cúm chỉ bằng 1/3 giá thuốc nhập khẩu

Theo báo cáo của IVAC, nhờ sự hỗ trợ của nhiều cơ quan, tổ chức trong và ngoài nước, IVAC đã nghiên cứu thành công vaccine cúm mùa (với ba chủng A/H1N1, A/H3N2 và cúm B) và vaccine cúm đại dịch A/H5N1. Công suất vaccine cúm mùa là 1,5 triệu liều/năm; vaccine cúm A/H5N1 là ba triệu liều/năm.
 
Phó Giáo sư, Tiến sĩ Lê Văn Bé, Viện trưởng IVAC cho biết, từ năm 2007, Việt Nam trở thành thành viên của Kế hoạch hành động toàn cầu về vaccine cúm của WHO. Năm 2010, WHO và một số tổ chức khác đã hợp tác với Việt Nam xây dựng kế hoạch dài hạn về sản xuất và sử dụng vaccine cúm; hướng dẫn thử nghiệm lâm sàng và hướng dẫn đăng ký vaccine cúm qua sử dụng công nghệ trứng gà có phôi.
 
Từ năm 2012 đến 2018, IVAC bắt đầu công tác thử nghiệm lâm sàng các loại vaccine cúm mùa và cúm A/H5N1 với nhiều giai đoạn. Kết quả tổng thể cho thấy, các vaccine được dung nạp tốt và có khả năng tạo đáp ứng miễn dịch bảo vệ. Hiện tại, IVAC đang thực hiện các thủ tục đăng ký cấp phép cho các loại vaccine trên; dự kiến sẽ lưu hành vào năm 2019; với giá thành chỉ bằng 1/3 so với giá thuốc nhập khẩu.
 
Theo IVAC, tại Việt Nam, mỗi năm có khoảng từ 1,2 đến 1,5 triệu người mắc hội chứng cúm, trong số đó 20-30% do vi-rút cúm mùa gây ra và dịch cúm gia cầm đã xuất hiện từ năm 2003. Trong khi đó, từ trước tới nay, Việt Nam luôn thiếu nguồn cung cấp vaccine cúm bền vững, buộc phải dựa vào nguồn thuốc nhập từ nước ngoài.
 
Nguồn: nhandan.com.vn

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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
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