GMPc Vietnam JSC
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Phong tê thấp Hoàng Xuân và loạt sản phẩm của Dược phẩm Khải Hà bị đình chỉ lưu hành

09/04/2018 | 1622 | Tin tức Tổng hợp

Do không đáp ứng quy định về ghi nhãn mỹ phẩm, sản phẩm Phong tê thấp Hoàng Xuân của Dược phẩm Khải Hà và 3 sản phẩm khác cũng của công ty này bị Cục Quản lý Dược (Bộ Y tế) bị đình chỉ lưu hành toàn quốc.

Trong công văn gửi tới Sở Y tế các tỉnh, thành phố trực thuộc trung ương và các đơn vị có liên quan, Cục Quản lý Dược thông báo, sản phẩm Phong tê thấp Hoàng Xuân do Công ty cổ phần Thương mại Dược VTYT Khải Hà sản xuất không đáp ứng quy định về ghi nhãn mỹ phẩm. Cục Quản lý Dược yêu cầu đình chỉ lưu hành trên toàn quốc sản phẩm này.
 
 Sản phẩm Phong tê thấp Hoàng Xuân bị đình chỉ do ghi nhãn sản phẩm không đúng quy định
 
Bên cạnh đó, còn có sản phẩm Bột ngâm chân Phong thấp của Dược Khải Hà, nước tắm Herbal do  Công ty TNHH Dược Minh Châu, sản phẩm Abby do Công ty cổ phần EU Pharma Việt Nam chịu trách nhiệm đưa ra thị trường bị đình chỉ vì sai phạm tương tự.
 
Được biết, cả 4 sản phẩm nói trên đều do Công ty cổ phần Thương mại Dược VTYT Khải Hà sản xuất.
 
Theo công văn từ Cục Quản lý Dược, các công ty chịu trách nhiệm đưa sản phẩm ra thị trường phải gửi thông báo thu hồi tới những nơi phân phối, sử dụng 4 sản phẩm nêu trên; thu hồi toàn bộ các lô mỹ phẩm không đáp ứng quy định; gửi báo cáo thu hồi các lô mỹ phẩm không đáp ứng quy định về Cục Quản lý Dược trước ngày 10/5.
 
Bên cạnh đó, Cục Quản lý Dược yêu cầu Sở Y tế tỉnh Thái Bình, Sở Y tế Thanh Hóa, Sở Y tế Hà Nội kiểm tra, giám sát thu hồi các mỹ phẩm do Công ty cổ phần Thương mại Dược VTYT Khải Hà sản xuất; báo cáo kết quả về Cục Quản lý Dược.
 
Nguồn: vtc.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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