GMPc Vietnam JSC
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Thông tư 31/2014/TT-BYT quy định về hồ sơ mời thầu thuốc

08/12/2014 | 1252 | Tin tức Tổng hợp

Ngày 26/09/2014, Bộ Y tế đã ban hành Thông tư 31/2014/TT-BYT về việc quy định bảng tiêu chuẩn đánh giá về mặt kỹ thuật tại hồ sơ mời thầu mua thuốc. Theo đó, phương pháp đánh giá sẽ được thực hiện theo phương pháp chấm điểm với thang điểm tối đa là 100 điểm.

Trong đó, chất lượng thuốc chiếm tối đa 70 điểm với các tiêu chí như: Cơ sở sản xuất mặt hàng thuốc tham dự thầu (25 điểm); tình hình vi phạm chất lượng của mặt hàng thuốc dự thầu (10 điểm); tình hình vi phạm chất lượng của cơ sở sản xuất mặt hàng thuốc dự thầu (10 điểm); hạn dùng của thuốc (10 điểm)… Đóng gói, bảo quản, giao hàng chiếm 30 điểm, gồm các tiêu chí: Cơ sở cung ứng mặt hàng thuốc (5 điểm); kinh nghiệm cung ứng thuốc của nhà thầu (5 điểm); khả năng đáp ứng yêu cầu của nhà thầu về điều kiện giao hàng (3 điểm)… 

Dựa vào thang điểm nêu trên, hồ sơ đề xuất được đánh giá đáp ứng yêu cầu về kỹ thuật khi có điểm của từng tiêu chí tại yêu cầu về chất lượng thuốc và đóng gói, bảo quản, giao hàng không thấp hơn 60% điểm tối đa của tiêu chí đó; đồng thời tổng điểm của tất cả các tiêu chí đánh giá không thấp hơn 80% tổng số điểm. 

Thông tư này có hiệu lực thi hành kể từ ngày ký; tuy nhiên đối với những hồ sơ mời thầu phát hành trước ngày 15/08/2014, việc đánh giá lựa chọn nhà thầu được thực hiện theo Thông tư số 37/2013/TT-BYT ngày 11/11/2013; những hồ sơ mời thầu phát hành sau thời điểm này nhưng nội dung hồ sơ mời thầu chưa phù hợp thì đơn vị phát hành hồ sơ mời thầu phải tiến hành sửa đổi để đảm bảo không trái với quy định của Thông tư này.

Xem toàn bộ Thông tư tại đây
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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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