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

Bán thuốc cao hơn giá đã kê khai, Dược phẩm Đông Phương bị phạt nặng

22/01/2018 | 475 | Tin tức Tổng hợp

Thanh tra Bộ Y tế vừa qua quyết định xử phạt Công ty TNHH Thương mại Dược phẩm Đông Phương với số tiền lên đến 30 triệu đồng vì vi phạm trong kinh doanh thuốc.
 
Bán thuốc cao hơn giá đã kê khai, Dược phẩm Đông Phương bị phạt nặng
 
Cụ thể, theo văn bản số 15/QĐ - XPVPHC của Thanh tra Bộ Y tế, Công ty TNHH Thương mại Dược phẩm Đông Phương (quận 7, TP. Hồ Chí Minh) bị xử phạt hành chính 30 triệu đồng do đã có hành vi bán thuốc Lacbio Pro số đăng ký VN - 11522 - 10 có giá cao hơn so với giá bán buôn dự kiến do Công ty Cổ phần Dược phẩm Bidiphar 1 đã kê khai theo quy định.
 
Hành vi của Công ty TNHH Thương mại Dược phẩm Đông Phương, theo Thanh tra Bộ Y tế cho biết là đã vi phạm quy định tại Điểm C, khoản 1, điều 47, Nghị định số 176/2013/NĐ - CP ngày 14/11/2013 của Chính phủ về quy định xử phạt vi phạm hành chính trong lĩnh vực y tế.
 
Ngoài phạt tiền, Công ty TNHH Thương mại Dược phẩm Đông Phương còn bị Thanh tra Bộ Y tế yêu cầu khắc phục hậu quả bằng cách buộc hoàn trả toàn bộ số tiền chênh lệch cho các khách hàng số tiền là  trên 62,3 triệu đồng.
 
Cũng liên quan đến vấn đề xử phạt trong lĩnh vực kinh doanh thuốc, Thanh tra Bộ Y tế vừa có quyết định số 16/QĐ – XPVPHC về việc xử phạt hành chính Công ty Cổ phần Đông dược Á Châu (quận Hà Đông, Hà Nội) số tiền 15 triệu đồng do có hành vi kinh doanh thuốc Hoàn sáng mắt ACP, số đăng ký V1350 - H12 - 10 khi không có giấy chứng nhận đủ điều kiện kinh doanh thuốc.
 
Theo Thanh tra Bộ Y tế, hành vi này của Công ty Cổ phần Đông dược Á Châu vi phạm quy định tại Điểm B, Khoản 2, Điều 37, Nghị định số 176/2013/NĐ - CP ngày 14/11/2013 của Chính phủ về quy định xử phạt vi phạm hành chính trong lĩnh vực y tế.
 
Nguồn: anninhthudo.vn

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