Key Benefits:
(The 22th ordinary meeting of the People's Government of Chilin Province, 10 October 2004, considered the adoption of the Decree No. 170 of 21 October 2004 of the People's Government Order No. 170 of 21 October 2004, which came into force on 1 December 2004) Article 1, in order to enhance the management of health supplies, ensure the effectiveness, quality and safety of health supplies, preserve the legitimate rights and interests of consumers and develop this approach in line with relevant national legislation, regulations. Article II refers to health supplies as a product that regulates human functions and promotes health. However, laws, administrative regulations and regulations such as medicine, health food, special-purpose dowry, medical equipment, sports, etc. have explicitly regulated the products specified. Article 3. This approach applies to units and individuals involved in the production of health supplies within the province's administration and to related administrative activities. Article 4 Other management of health supplies is managed in accordance with their respective responsibilities. The production of health-care supplies is subject to approval certificates and classification management systems. The Health Productive Approval Certificate in Glin Province was issued by the Provincial Health Administration for a five-year period to be reviewed annually. The units and individuals that have not obtained the certificates for the production of health supplies in the provinces of Glinh shall not engage in productive activities in the name of health supplies. The types of health supplies are determined by the provincial health administration and are made available to society in a timely manner. Article 6. (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) The existence of plant or premises that are adapted to product varieties, quantity and quantity; (iv) The production facilities that are suitable for product characteristics for the production of vehicles, which are consistent with health requirements; (v) Place health permits granted by the municipal health administration at the enterprise location (release). Article 7 units and individuals applying for the Certificate of Production of Health Goods in the Province of Glinin must have the health conditions set out in article 6 of this approach and provide the provincial health administration with the following materials: (i) Three applications; (ii) Product production patterns, formulations or construction, production processes and quality standards; (iii) Safety evaluation of raw materials and products; (iv) Evaluation of product health functions; (v) Product samples; (vi) A description of product labelling and product use. Article 8. The provincial health administration should be completed within 15 working days from the date of receipt of the request. In accordance with conditions, they are approved and issued for the approval of the certificate; they are not subject to conditions, are not approved, justifying the reasons and notify the applicant in writing. The units and individuals applying for the GREPS certificates should also be subject to the procedures for the operation of health-care supplies in the pre-approved business administration. Article 9. The certificates for the production of health supplies in the Ghlin province expired on 30 days before the date of entry by the licensee for the conversion of approval certificates to the original approval authority and the late application of the original approval certificate. Article 10. The provincial health administration has established a health supplies assessment committee composed of experts responsible for the effectiveness, health standards and safety evaluation of health supplies in the province and for evaluation reports. Health supplies should be detected by law. The testing is carried out by the mandated inspection body. Monitoring results should be reported by the detection body. Article 11 prohibits the conversion, sale, rental and loan of a certificate of approval for the production of health supplies in Glin. The producers of health-care supplies shall not be allowed to change their ownership of products approved by the Provincial Health Administration, production processes, quality standards, product name, product labelling and use statements. There is a need for change and approval by the author's approval authority. Article 13 Use of statements and labels for health supplies should indicate the name of the product, the place of the plant, the place of the plant and the production of approval. Indirect packaging should indicate the date of production, the time period for effective use, the main components, the role of health care, the subject of application, and health supplies that may give rise to adverse reactions should also be noted. Article 14. The content of statements of use of health supplies, small packaging, labelling and advertising must be authentic, legitimate, scientific, consistent with product quality requirements and national and local quality management provisions and should not be mistreated and misleading. Article 15. Health supplies should be printed in out-of-product packaging (including labelling, use of notes, etc.) in “Highforests for health supplies”. Article 16 states that the provincial health administration should conduct regular monitoring of health supplies with the relevant administration and make the findings available to society. Article 17, in violation of this approach, provides that one of the following acts is rectified by an order of responsibility for the health administration at the district level and a fine of more than 1000 dollars: (i) No certificate of approval for the production of health supplies in Glin Province; (ii) Removal or other unjustifiable means of obtaining a certificate of approval for the production of health supplies in Glin Province. In violation of this approach, the production of non-qualified health supplies is punishable by law by the Ministry of Business Administration, Quality Technical Monitoring. Article 19, in violation of this approach, provides that one of the following acts is recovered by the health administration at the district level by the approval for the production of health supplies in the provinces of Glin and fined by more than 1000 dollars: (i) Restructuring, selling, renting and borrowing from the Approval of Health Productive Products in Glin Province; (ii) Remove unauthorized changes in the distribution of products approved by the Provincial Health Administration, production processes, quality standards, product name, product labelling and use of notes. Article 20 Business in the production of health supplies violates laws, regulations and regulations, such as the Drugs Management Act, the Product Quality Act, the Stockpile Health Monitoring Regulations, and is punishable by law by the relevant authorities such as food medicine surveillance, quality technical supervision, and business administration. Article 21, where the parties are not guilty of administrative penalties, may apply for administrative review or administrative proceedings in accordance with the law. Article 22 staff members of the executive organs, in monitoring management, abuse of their functions, insistance, in favour of private fraud, are administratively disposed of by their units or at the superior authorities; and constitute criminal liability by law. Article 23 of this approach is implemented effective 1 December 2004. |
