(Adopted at the 8th ordinary meeting of the People's Government of Honour, 16 September 2008, No. 108, dated 24 September 2008, on the date of publication, on the date of publication, of the People's Government Order No. 108,

Article 1. To strengthen the monitoring of health supplies, to preserve the legitimate rights and interests of consumers, and to develop this approach in line with the relevant laws, regulations.

Article 2 refers to health-care supplies, which are directly or indirectly instrumental in the physical surface, not for the purpose of treating diseases, indicating products with specific health functions. However, the laws, regulations provide for other provisions, such as medicine, medical equipment, health food, special-purpose steriles, sterilization products, sports agents.

Article 3. This approach applies to the production, sale and management of health supplies within the territorial administration.

Article IV. The Government's Health Administration is responsible for the management of health-care supplies throughout the province and is responsible for the approval of health permits for health supplies.

The Government of the city (State, land) and the Government's Health Administration at the district level are responsible for the management of health-care supplies in this administrative area.

The administration of health supplies is responsible for the management of health supplies within their respective responsibilities.

Article 5 imposes a health permit system for health supplies.

Article 6. The applicant shall have the following conditions:

(i) The construction of enterprises in clean areas and the maintenance of intervals with toxic and harmful sites consistent with health requirements;

(ii) The plant should be solid and clean. In the course of the workshop, the walls, the use of photocetic building materials on the ground, the extraction of light or the goodness of lighting, the facilities and measures that prevent and eliminate rats and other harmful pyrethroids;

(iii) There are plants or places that are adapted to the production, packaging, storage, etc. of health supplies;

(iv) The production facilities that are suitable for product characteristics for the production of vehicles, which are consistent with health requirements;

(v) Professional technicians with health management systems and access to health certificates.

The applicant shall provide the following information to the Government's Health Administration:

(i) An application form;

(ii) Product development reports, naming, grouping base and relevant information;

(iii) Product production processes;

(iv) Quality criteria for products;

(v) Recent product-based testing reports for products samples and those with test qualifications;

(vi) A compilation, labelling and presentation of products.

Article 7. Upon receipt of the request by the Government of the Provincial People's Health Administration, a health supplies evaluation board consisting of specialists such as medical, secondary, toxic, nutrition, testing, medical equipment, production process, management, standard use, and evaluation of the stereotypes, production processes, health efficiency and safety of health supplies and evaluation reports.

Article 8. The Government's Health Administration shall take a decision within 15 days of the date of receipt of the evaluation report of the Committee on the Assessment of Health Goods. The evaluation report determines that it is in accordance with the conditions of the licence, gives a health licence for health supplies; the evaluation reports determine that the licence is not in accordance with the conditions of the licence, the decision to be taken without the licence and the reasons for the written statement.

Article 9

Contraints are prohibited, sold, rented and licensed health supplies.

Article 10 Use of statements and labels of health supplies should indicate the name of products, the place of the plant, the factory and the health-care supply licence number; minor packaging or the use of statements should indicate the date of production, the duration of use, the main ingredients, the role of health, the subject of application, and the possible adverse response, and the use of methods and concerns should also be noted.

The labelling of health supplies, small packaging or use of notes shall not be construed as a result of adaptation, and shall not promote the effectiveness of the treatment and shall not use medical terminology.

Article 11. The sales of health supplies shall not sell unqualified, unqualified, expired health supplies.

Article 12 does not obtain health permits for the production of health-care supplies, which are warned by the Government's health administration at the district level and fined by over 3,000 dollars. Without the proceeds of the offence, the penalty of more than 5,000 is imposed.

Article 13, in violation of article 9 of this approach, is warned by the Government's health administration at the district level and fined by more than 5,000.

Article 14. In violation of article 10 of this approach, the Government's health administration, at the district level, has given warning that the period of time has been changed; the period of time has not been changed, with a fine of over 5,000 dollars.

Article 15, in violation of article 11 of this approach, is punishable by law by the Ministry of Business Administration and the quality of products.

Article 16 Abuses of duties, omissions, provocative fraud by staff of the health administration and other relevant departments are not yet criminalized, and administrative disposal is granted to the competent and other direct responsible persons directly responsible.

Article 17