GMPc Vietnam JSC
  • 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

    News

  1. Home
  2. News
  3. Tin tức Tổng hợp

News category

  • GMPC News
    • Notification
    • Activities & Cooperation
    • Internal News
  • Field News
    • Exhibition & Conference
    • News
    • Typical GMP enterprise
  • GMP Projects News
    • GMPc contract
    • Project Progress Updates

'Chợ' dược phẩm lớn nhất Hà Nội bán hàng không nguồn gốc

20/08/2015 | 919 | Tin tức Tổng hợp

Mục lục nội dung

    Bất ngờ kiểm tra các quầy thuốc tại trung tâm phân phối dược phẩm lớn nhất Hà Nội (số 1 Nguyễn Huy Tưởng, Thanh Xuân, HN), cơ quan chức năng đã phát hiện hàng ngàn sản phẩm bày bán ở đây không rõ nguồn gốc.
     

    Sáng 18/8, 4 đội cơ động thuộc Chi cục Quản lý thị trường Hà Nội (QLTT) đồng loạt kiểm tra các quầy thuốc tại Trung tâm phân phốidược phẩm và trang thiết bị y tế Hapu (địa chỉ số 1 Nguyễn Huy Tưởng, Thanh Xuân, Hà Nội).
    Nhiều sai phạm tại trung tâm mệnh danh “chợ” dược phẩm, trang thiết bị y tế lớn nhất thủ đô đã bị cơ quan chức năng phát hiện. Cụ thể, qua kiểm tra 9 quầy thuốc do các đơn vị kinh doanh dược thuê địa điểm, có đến 8 quầy vi phạm kinh doanh, như: Trang thiết bị y tế do nước ngoài sản xuất không có hóa đơn chứng từ chứng minh nguồn gốc. Thậm chí, một số sản phẩm không có số đăng ký lưu hành. Trong đó, có 1.000 chai nước hồng sâm, 75 cuộn băng lụa dùng trong y tế, hơn 1.400 chiếc thông tiểu và 14 hộp thuốc nhãn Farmiga.
    Với những hành vi vi phạm trên, lực lượng QLTT Hà Nội đã tiến hành lập biên bản, tịch thu sản phẩm, buộc tiêu hủy và phạt hành chính tại chỗ các đơn vị này (tổng tiền phạt hơn 70 triệu đồng).
    Đội trưởng Đội QLTT số 1 Nguyễn Đăng Khoa cho biết: “Đây là một trong những trung tâm có cơ sở vật chất, cơ sở kinh doanh tương đối lớn. Việc kiểm tra, kiểm soát những cơ sở kinh doanh như thế này rất cần thiết. Không chỉ giai đoạn này mà còn là công việc thường xuyên của QLTT để phát hiện sai phạm về hàng giả, hàng lậu đối với mặt hàng dược phẩm, mỹ phẩm và thực phẩm chức năng”.
    Trao đổi với báo chí, ông Ngô Quốc Doanh, Phó TGĐ Cty CP Đầu tư Bất động sản Hapulico cho hay: “Khi bị cơ quan chức năng phát hiện sai phạm, chúng tôi cương quyết chấm dứt hợp đồng với các công ty kinh doanh thuốc trước thời hạn”.
    Theo kế hoạch, lực lượng chuyên ngành, liên ngành sẽ tiếp tục kiểm tra nhiều trung tâm, cơ sở kinh doanh thuốc, mỹ phẩm, thực phẩm chức năng khác trong thời gian tới.
    Theo CafeF 

    Related news

    Ground - Breaking ceremony of HSC - HOSTEP stem cell technology complex

    Ground - Breaking ceremony of HSC - HOSTEP stem cell technology complex

    09/01/2025 | 355

    Hòa Lạc Stem Cell Technology Joint Stock Company (HSC) begins construction of the HSC HOSTEP Stem Cell Technology Complex according to...

    What is quality risk management in pharmaceutical?

    What is quality risk management in pharmaceutical?

    07/12/2023 | 60

    Quality risk management in pharmaceutical is a systematic process for the assessment, control, communication and review of risks to the quality of...

    The Guide to creating a GMP Training Program

    The Guide to creating a GMP Training Program

    04/12/2023 | 50

    GMP training is an informational program that covers the required guidelines for your industry. Your GMP training will be required to cover...

    GMP training for employees – essential steps

    GMP training for employees – essential steps

    04/12/2023 | 20

    In principle, the GMP training program can be built around the following steps with clear objective and deliverables. The training program should...

    How to conduct GMP training for employee

    How to conduct GMP training for employee

    04/12/2023 | 38

    A successful GMP training for employee ensures that all staff will receive adequate, relevant and documented training to enable them to perform...

    Internal audits, Complaints, Product Recalls in GMP

    Internal audits, Complaints, Product Recalls in GMP

    06/11/2023 | 32

    Pharmaceutical manufacturers regularly conduct internal audits which is a way of verifying that all quality related activities comply with the code of...

    • 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
    • Email: contact@gmp.com.vn
    • Representative Office: 156/1/1, Cong Hoa Street - Ward 12 - Tan Binh District - Ho Chi Minh City
    • Tel: 0283.811.7383 
    • Quick link
    • About Us
    • Services
    • Project
    • GMP-Handbook
    • Video
    • Consulting for cosmetic facility
    • Consulting for health supplement facility
    • Consulting for GSP warehouse
    • Fanpage
    Facebook

    Copyright © 2020 GMPc. All rights reserved.

    • 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
    Nhắn tin Facebook Zalo: 0982.866.668