Decision No. 108/2002/QĐ-TTg On approving the strategy for the development of the pharmaceutical industry until 2010

Decision No. 108/2002/QĐ-TTg approves the Strategy for the Development of the Pharmaceutical Industry until 2010, with the goal of industrializing and modernizing the pharmaceutical industry, ensuring the supply of high-quality drugs, rational and safe drug use. The strategy includes solutions related to planning, technology, human resources, quality management, investment policies, and finance.

문서 번호108/2002/QĐ-TTg
문서 유형Decision
발행 기관Ministry of Health
서명자Phạm Gia Khiêm — Phó Thủ tướng
업데이트30. 06. 2026
산업Health
분야Pharmaceuticals and Cosmetics
발행일15. 08. 2002
발효일30. 08. 2002
효력 만료일31. 12. 2013
상태Expired
✦ 스마트 요약

Decision No. 108/2002/QĐ-TTg approves the Strategy for the Development of the Pharmaceutical Industry until 2010, with the goal of industrializing and modernizing the pharmaceutical industry, ensuring the supply of high-quality drugs, rational and safe drug use. The strategy includes solutions related to planning, technology, human resources, quality management, investment policies, and finance.

핵심 사항

  • The pharmaceutical industry will be developed into a leading economic-technical sector, industrialized and modernized, ensuring the supply of high-quality drugs (Article 1.2.a)
  • All production, business, research, and testing facilities for pharmaceutical products must meet GMP standards by 2010 (Article 1.2.a)
  • Enhance drug production capacity in terms of scale and quality, invest in advanced technology production lines (Article 1.3.a)
  • Focus on training pharmaceutical human resources, develop retail networks, particularly in remote areas (Article 1.3.b)
  • Modernize the drug quality assurance system and establish preferential policies for enterprises investing in research and technological innovation (Article 1.4.d)

🌐 이 문서의 사회적 영향

  • Positive impact: Increase the supply of high-quality drugs, promote rational and safe drug use, and develop the pharmaceutical industry into a leading economic sector.
  • Negative impact: Investment costs for advanced technology and human resource training may increase, affecting small and medium-sized enterprises.

❓ 자주 묻는 질문

Who does this strategy apply to?

This strategy does not specify specific target groups but will be implemented by state agencies responsible for pharmaceuticals, enterprises, and citizens.

What are the specific goals by 2010?

By 2010, all production, business, research, and testing facilities for pharmaceutical products will meet GMP standards (Article 1.2.a).

Where will modern technology be invested?

Modern technology will be invested in drug production lines, especially essential drugs and herbal medicines (Article 1.3.a).

What is the source of funding for implementing this strategy?

Funding sources include the state budget, bilateral and multilateral cooperation, foreign direct investment, domestic enterprise capital, and community contributions (Article 1.5.c).

How long is the implementation period for this strategy?

The strategy is divided into two phases: from 2002 to 2005 and from 2006 to 2010 (Article 1.5.e).

전문

 

 

DECISION OF THE PRIME MINISTER

Regarding the approval of

Strategy for the Development of the Pharmaceutical Industry to 2010

_________________________

PRIME MINISTER 

Pursuant to the Law on Organization of the Government dated December 25, 2001;

Pursuant to the Public Health Law dated July 30, 1989;

At the request of the Minister of Health in the report No. 3880/TTr-BYT dated May 17, 2002,

 

DECISION:

Article 1.Approves the "Strategy for the Development of the Pharmaceutical Industry to 2010" with the following main contents:

1. General objectives:

Develop the pharmaceutical industry into a leading economic-technical sector towards industrialization-modernization, actively integrating regionally and globally to ensure a steady supply of quality medicines, ensuring rational and safe drug use, serving the health care and protection of the people's health.

2. Specific objectives By 2010:

a) Invest in modern technology, update equipment and management systems so that the pharmaceutical industry gradually meets raw material needs. By the end of 2010, all production, trading, research, and testing facilities for pharmaceuticals will meet Good Practice (GP) standards.

b) Build industrial bases for antibiotic and chemical drug production, producing raw materials for drugs with strengths, especially from medicinal herbs.

c) Ensure a steady supply of quality medicines without shortages of essential drugs, drugs for national health programs (malaria prevention, tuberculosis prevention, goiter prevention, etc.). Pay special attention to ensuring adequate drug supply services for people in difficult areas.

d) Ensure rational, safe, and effective drug use.

đ) Ensure domestic production of 60% of the society's demand for disease-prevention and treatment drugs; average drug consumption reaches 12-15 USD/person/year; have 1.5 pharmacists with advanced degrees per 10,000 people.

3. Main solutions and policies:

a) Solutions on planning, technological innovation, and scientific research:

Plan the pharmaceutical industry towards industrialization-modernization and international integration. Enhance drug production capacity in scale and quality, invest in high-tech production lines to leapfrog development. Plan and modernize the drug distribution system including import-export, wholesale, and retail. Develop retail networks, focusing on remote, mountainous, and island regions.

Prioritize investment in chemical production facilities and raw material sources. Focus on producing essential drugs, export-oriented drugs, drugs from medicinal herbs, and generic drugs replacing imported ones; research and produce various formulations for children and the elderly. Emphasize investment in developing medicinal herbs.

Develop scientific research on drug formulation technology, biotechnology, medicinal herbs, and drug analysis to serve the production of new drugs. Vigorously apply information technology to management, production control, drug supply, and usage...

Closely integrate human resources and equipment in the pharmaceutical industry with those of other ministries, research institutes, and scientific centers to conduct drug and raw material research, linking research processes with the practical production of pharmaceutical enterprises.

b) Solutions on organization and human resource development:

Strengthen and enhance the state management system for pharmaceuticals: Improve the Vietnam National Pharmaceutical Administration; reorganize and strengthen specialized pharmaceutical inspection; complete the organizational structure of pharmaceutical management departments at provincial health bureaus; plan the pharmaceutical production system.

Emphasize pharmaceutical human resource training: Increase training and retraining of various types of pharmaceutical staff. Develop postgraduate education. Identify and nurture talents, train high-level research personnel. Establish new pharmacy departments at medical universities to train pharmacists for difficult areas.

Train and rationally utilize pharmaceutical human resources, implement dispatch and targeted training to address imbalances in pharmaceutical personnel between regions, particularly ensuring sufficient pharmaceutical staff for mountainous, remote, and rural areas.

c) Solutions on drug quality monitoring:

Modernize the drug quality assurance system.

Reorganize the state drug quality inspection system. Enhance the capacity of drug testing laboratories to test circulating pharmaceutical products.

Create conditions and encourage the establishment of modern external drug testing service facilities outside the state system.

d) Solutions on policy and mechanism building:

Complete the legal system for pharmaceutical management. Draft the Pharmaceutical Law. Amend, supplement, and promulgate new regulatory documents on pharmaceuticals, regulations, technical norms, and standards. Standardize pharmaceutical management, production, and supply activities, moving towards international standards.

Develop preferential policies for businesses investing in research and development, technological innovation, raw material production, and export product manufacturing.

Develop policies to encourage foreign investment in the pharmaceutical industry, prioritizing projects for raw material production, especially those using high-tech and biotechnology. Implement appropriate policies for foreign investment in the drug distribution sector.

Diversify pharmaceutical business models, accelerate the process of shareholding. Encourage businesses to enhance research capabilities to create new products.

Strengthen cooperation with countries in the region and worldwide, with the World Health Organization and other international organizations. Implement an appropriate economic integration roadmap consistent with bilateral and multilateral commitments, gradually harmonizing pharmaceutical regulations with regional and global standards.

Direct and promote rational, safe, and effective drug use as a key and ongoing task of the healthcare sector. Limit and gradually reduce the misuse of drugs, particularly antibiotics, corticosteroids, vitamins, and brand-name drugs. Encourage the use of generic drugs, domestically produced drugs, and traditional medicine.

d) Ensure financial resources:

Maximize and effectively utilize funds from the state budget, bilateral and multilateral cooperation funds from non-governmental organizations, foreign investment, domestic enterprises, and community resources.

The central State budget sources shall be allocated for scientific research needs, human resource training, herbal potential development and raw material pharmaceutical industry development, investment in public enterprises, and enhancing the capacity of State management agencies and testing agencies.

Foreign investment sources shall focus on the pharmaceutical production sector, encouraging investment in modern technology production lines, prioritizing raw material pharmaceutical production.

Investment demands for developing pharmaceutical production and business operations of enterprises shall be mobilized from loan capital, own capital, shareholding...

Based on the implementation plan of the Strategy, the Ministry of Health will prepare a budget estimate to send to the Ministry of Finance, the Ministry of Planning and Investment for review, balance, and inclusion in the annual budget report to the Government for submission to the National Assembly for approval.

e) Implementation period of the Strategy:

From 2002 to 2010, divided into two phases:

Phase 1: from 2002 to 2005

Phase 2: from 2006 to 2010

Based on actual conditions, the Ministry of Health will develop specific plans and targets for each phase, aligning with the contents of this Strategy.

Article 2.The Ministry of Health shall take the lead, coordinate with the Ministry of Planning and Investment, the Ministry of Finance, and relevant ministries and sectors to develop plans, guide inspections, monitor, and compile annual implementation status reports of the Strategy to report to the Prime Minister; organize mid-term reviews of the Strategy in 2005 and final reviews of the Strategy in 2010.

Article 3. This Decision shall take effect fifteen days from the date of signature.

Article 4. Ministers, heads of ministerial-level agencies, heads of government-affiliated agencies, Chairpersons of People's Committees of provinces and centrally governed cities are responsible for implementing this Decision./.

 

 

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관계도

108/2002/QĐ-TTg
Decision No. 108/2002/QĐ-TTg On approving the strategy for the development of the pharmaceutical industry until 2010
Expired
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관련 5
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