GMPc Vietnam JSC
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Tăng cường xử lý vi phạm trong kinh doanh thực phẩm chức năng

24/04/2020 | 340 | Tin tức Tổng hợp

Thủ tướng Chính phủ yêu cầu Bộ Y tế tăng cường công tác thanh tra, kiểm tra, xử lý vi phạm trong kinh doanh, quảng cáo thực phẩm chức năng.
 
Tăng cường xử lý vi phạm trong kinh doanh thực phẩm chức năng

Ngày 13-4, Thủ tướng Chính phủ ban hành Chỉ thị 17/CT-TTg về việc tiếp tục tăng cường trách nhiệm quản lý nhà nước về an toàn thực phẩm (ATTP) trong tình hình mới.
 
Trong thời gian qua, công tác bảo đảm ATTP tạo được những chuyển biến rõ rệt, tích cực trên toàn diện các lĩnh vực do nhận được sự quan tâm lãnh đạo, chỉ đạo của cả hệ thống chính trị từ trung ương đến địa phương. Những vấn đề gây bức xúc dư luận xã hội đã được kiểm soát giảm cả số lượng, mức độ và hiện tượng.
 
Tuy nhiên, công tác bảo đảm ATTP vẫn còn khó khăn, thách thức do sản xuất nhỏ lẻ vẫn còn nhiều. Thói quen lạm dụng, sử dụng thuốc bảo vệ thực vật, vật tư nông nghiệp không đúng quy trình, không rõ nguồn gốc còn khá phổ biến. Quản lý hoạt động giết mổ gia súc, gia cầm nhỏ lẻ với nhiều nguy cơ không bảo đảm an toàn còn khó khăn. Việc kinh doanh, quảng cáo thực phẩm chức năng vi phạm pháp luật, đặc biệt trên mạng xã hội diễn biến phức tạp, khó quản lý…
 
Chính vì thế, để tiếp tục nâng cao hiệu lực, hiệu quả công tác quản lý, bảo đảm ATTP, Thủ tướng Chính phủ yêu cầu Bộ Y tế chủ trì, tiếp tục nghiên cứu hoàn thiện thể chế quản lý ATTP phù hợp với thông lệ quốc tế, đáp ứng yêu cầu hội nhập. Đồng thời tăng cường công tác thanh tra, kiểm tra, xử lý vi phạm trong kinh doanh, quảng cáo thực phẩm chức năng, phụ gia thực phẩm, chất hỗ trợ chế biến thực phẩm…
 
Bên cạnh đó, Thủ tướng Chính phủ yêu cầu các bộ, cơ quan ngang bộ, UBND các cấp thực hiện nghiêm túc, đầy đủ trách nhiệm quản lý ATTP; tăng cường công tác hậu kiểm, thanh tra, kiểm tra và xử lý nghiêm, kể cả về hình sự các tổ chức, cá nhân vi phạm nghiêm trọng các quy định về ATTP, gây ảnh hưởng tới sức khỏe người tiêu dùng theo quy định của pháp luật. Xử lý nghiêm tổ chức, cá nhân lơ là, thiếu trách nhiệm trong quản lý ATTP…
Nguồn: plo.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
 
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