GMPc Vietnam JSC
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    • CGMP, ISO 22716-certified cosmetics facilities  
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    • Health-supplement facilities  
      • Project feasibility study
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      • Detail Construction and MEP drawing
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      • HS GMP Training and Guidance
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      • HS GMP - Re-evaluation consultation
    • Eligibility For Cosmetic Manufacturing  
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      • Detail Construction and MEP drawing
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      • Feasibility Study
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      • GSP registration and operation consultancy
    • GSP warehouses  
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      • Detail Construction and MEP drawing
      • GSP Training and Guidance
      • Overall Consultation on Designing And Constructing
      • GSP Re-evaluation consultation
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      • 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
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Cục Quản lý Dược thu hồi 9 loại thuốc kém chất lượng

18/11/2019 | 159 | Tin tức Tổng hợp

Danh sách 9 loại thuốc kém chất lượng bị Cục Quản lý Dược (Bộ Y tế) ra thông báo thu hồi có 5 công ty của Việt Nam, 2 công ty của Ấn Độ, 1 công ty đến từ Thái Lan và 1 công ty đến từ Hàn Quốc.
 
Cục Quản lý Dược (Bộ Y tế) vừa công bố danh sách 9 công ty và tên thuốc kém chất lượng đã bị Cục thông báo thu hồi trong năm 2019.
 
Các thuốc bị thu hồi thuộc nhóm thuốc với công dụng quen thuộc, ví dụ kháng viêm (Cetirizine 10mg, Alphachymotrypsine 4200 đơn vị và Promethazin), kháng sinh (Acigmentin 375, AMK 625), thuốc tiêu hóa (Arpizol, Virvic gran), thuốc nội tiết (Methylprednisolone). Riêng Halaxamus là thuốc biệt dược.
 
Cục Quản lý Dược thu hồi 9 loại thuốc kém chất lượng
 
 Trong khi các thuốc của Việt Nam và Hàn Quốc vi phạm ở mức độ 2, không bảo đảm đầy đủ hiệu quả điều trị, hoặc không an toàn cho người sử dụng nhưng chưa đến mức gây tổn hại nghiêm trọng đối với sức khỏe, chưa ảnh hưởng đến tính mạng của người sử dụng, thì thuốc của Ấn Độ và Thái Lan chỉ vi phạm ở mức độ 3, tức là các thuốc này vi phạm nhưng không ảnh hưởng đến hiệu quả điều trị và an toàn khi sử dụng.
 
 
Thời gian qua, liên tiếp xuất hiện một số loại thuốc kém chất lượng bị Cục Quản lý Dược ra thông báo thu hồi.
 
Với việc công khai danh sách các thuốc vi phạm, người tiêu dùng có thể dễ dàng tra cứu, tránh mua phải các loại thuốc kém chất lượng này, đồng thời, giúp việc quản lý thuốc chặt chẽ, minh bạch hơn.
Nguồn: vietnamnet.vn

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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
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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
 
Hotline: 0982.866.668
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