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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      • HS GMP Training and Guidance
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      • HS GMP - Re-evaluation consultation
    • Eligibility For Cosmetic Manufacturing  
      • Overall consultation
      • Detail Construction and MEP drawing
      • Designing, Constructing, Ensured Certification
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      • Project feasibility study
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      • GSP Re-evaluation consultation
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      • Project Feasibility Study
      • Technology and Equipment consultation
      • Detail Construction and MEP Drawing
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      • WHO GMP Training and Guidance
      • Preparation of WHO GMP registration dossier
      • WHO GMP Re-evaluation consultation
    • GMP, GLP, GSP training  
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“Tiền mất tật mang” vì dược liệu nhập chui

04/10/2016 | 1504 | Tin tức Tổng hợp

Mỗi năm có khoảng 40.000 tấn dược liệu nhập chui vào Việt Nam đa phần là là dược liệu kém chất lượng hoặc đã bị chiết xuất một phần hoạt chất.

Theo ông Trương Quốc Cường, Cục trưởng Cục Quản lý Dược (Bộ Y tế), hơn 80% trong số 60.000 tấn dược liệu sử dụng mỗi năm tại Việt Nam là nhập khẩu. Đa số lại nhập theo con đường tiểu ngạch dưới dạng nông sản hoặc đăng ký sản xuất thực phẩm chức năng, mỹ phẩm nhưng lại được sử dụng để làm thuốc.

 
Nhiều loại dược liệu khi nhập khẩu không có bao bì, nhãn mác theo đúng quy định, phần lớn được đóng gói trong bao, thùng giấy, không kiểm tra được cụ thể các mặt hàng. Tại các cửa khẩu, cán bộ chỉ kiểm tra được số lượng, trọng lượng bao hàng, không kiểm tra được chất lượng các dược liệu.
 
Trong ki đó, từ tháng 3/2016 đến nay, Cục Quản lý Y dược cổ truyền mới cấp 14 giấy phép nhập khẩu dược liệu cho các công ty sản xuất dược tại Việt Nam, với tổng số 1.400 tấn dược liệu có nguồn gốc, xuất xứ rõ ràng được nhập khẩu vào trong nước. 
 
Năm 2015, Viện Kiểm nghiệm thuốc Trung ương phối hợp với Cục Y dược cổ truyền kiểm tra, khảo sát các loại dược liệu có nghi ngờ về chất lượng tại các bệnh viện y học cổ truyền và các công ty xuất nhập khẩu dược liệu trên toàn quốc.
 
Trong 109 mẫu được kiểm tra, phần lớn mẫu được lấy từ khu vực cửa khẩu biên giới với Trung Quốc, thì có đến 56 mẫu không đạt chất lượng, trong đó có đến 24 mẫu dược liệu giả mạo đã được đưa vào các cơ sở y tế công lập sử dụng.
 

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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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