(Promulgated by the State Council on May 21, 1987, and revised in accordance with the Decision of the State Council on Amending the Regulations on the Administration of Veterinary Drugs on November 29, 2001)Өгүүлэл нь ...-аас авсанFOFCC-http://fofcc.org.cn/mn/11220/
Chapter I General ProvisionsӨгүүлэл нь ...-аас авсанFOFCC-http://fofcc.org.cn/mn/11220/
Article 1 These Regulations are specially formulated in order to strengthen the supervision and administration of veterinary drugs, ensure the quality of veterinary drugs, effectively prevent and treat diseases of livestock, poultry and other animals, promote the development of the animal husbandry industry and safeguard human health.Өгүүлэл нь ...-аас авсанFOFCC-http://fofcc.org.cn/mn/11220/
Article 2 The production, operation and use of veterinary drugs must ensure quality and safety and efficacy.Өгүүлэл нь ...-аас авсанFOFCC-http://fofcc.org.cn/mn/11220/
Article 3 The administrative department of animal husbandry and veterinary medicine under the State Council shall be in charge of the administration of veterinary drugs throughout the country, and the administrative departments of animal husbandry and veterinary medicine of local people's governments at or above the county level shall be in charge of the administration of veterinary drugs within their respective jurisdictions.Өгүүлэл нь ...-аас авсанFOFCC-http://fofcc.org.cn/mn/11220/
Article 4 All those engaged in the production, operation and use of veterinary drugs shall comply with the provisions of these Regulations.Өгүүлэл нь ...-аас авсанFOFCC-http://fofcc.org.cn/mn/11220/
Chapter II Administration of Veterinary Drug Manufacturing EnterprisesӨгүүлэл нь ...-аас авсанFOFCC-http://fofcc.org.cn/mn/11220/
Article 5 Veterinary drug manufacturing enterprises must meet the following conditions:Өгүүлэл нь ...-аас авсанFOFCC-http://fofcc.org.cn/mn/11220/
(1) Having technical personnel and skilled workers with technical positions of engineer or veterinarian or above commensurate with the veterinary drugs to be produced;Өгүүлэл нь ...-аас авсанFOFCC-http://fofcc.org.cn/mn/11220/
(2) Having factory buildings, facilities and sanitary environment commensurate with the veterinary drugs to be produced;Өгүүлэл нь ...-аас авсанFOFCC-http://fofcc.org.cn/mn/11220/
(3) Having facilities and conditions conforming to the national standards for labor safety and hygiene;Өгүүлэл нь ...-аас авсанFOFCC-http://fofcc.org.cn/mn/11220/
(4) Having a quality inspection institution, full-time inspection personnel and necessary instruments and equipment;Өгүүлэл нь ...-аас авсанFOFCC-http://fofcc.org.cn/mn/11220/
(5) Enterprises not specializing in the production of veterinary drugs but concurrently producing veterinary drugs must have a separate veterinary drug production area.Өгүүлэл нь ...-аас авсанFOFCC-http://fofcc.org.cn/mn/11220/
Article 6 To establish a veterinary drug manufacturing enterprise, it must be examined and approved by the administrative department of animal husbandry and veterinary medicine of the county-level people's government where the enterprise is located, and upon examination and approval by the administrative department of animal husbandry and veterinary medicine of the people's government of the province, autonomous region or municipality directly under the Central Government, a Veterinary Drug Manufacturing License shall be issued. A veterinary drug manufacturing enterprise shall, with the Veterinary Drug Manufacturing License, apply to the local administrative organ for industry and commerce for registration, and upon approval, obtain a Business License.Өгүүлэл нь ...-аас авсанFOFCC-http://fofcc.org.cn/mn/11220/
The Veterinary Drug Manufacturing License shall specify a period of validity, and upon expiration, a new license shall be issued after re-examination and qualification.Өгүүлэл нь ...-аас авсанFOFCC-http://fofcc.org.cn/mn/11220/
Article 7 Veterinary drug manufacturing enterprises must conduct production in accordance with technical procedures, production records must be complete and accurate, and the required raw materials, auxiliary materials, and containers and packaging materials directly contacting veterinary drugs must meet pharmaceutical requirements.Өгүүлэл нь ...-аас авсанFOFCC-http://fofcc.org.cn/mn/11220/
Article 8 Veterinary drug packaging must bear a label indicating the words “For Veterinary Use” and be accompanied by instructions. The label or instructions must indicate the trademark, veterinary drug name, specifications, enterprise name, product batch number and approval number, and state the main ingredients, content, action, use, method of administration, dosage, period of validity and precautions of the veterinary drug.Өгүүлэл нь ...-аас авсанFOFCC-http://fofcc.org.cn/mn/11220/
Article 9 Subpackaging of veterinary drugs must have complete and accurate subpackaging records, and the packaging shall indicate the veterinary drug name, specifications, enterprise name, product batch number, approval number, subpackaging unit and subpackaging batch number, and be accompanied by instructions. For veterinary drugs with a specified period of validity, the period of validity must be indicated after subpackaging.Өгүүлэл нь ...-аас авсанFOFCC-http://fofcc.org.cn/mn/11220/
Article 10 Veterinary drugs must undergo quality inspection before leaving the factory, and those not conforming to quality standards shall not leave the factory.Өгүүлэл нь ...-аас авсанFOFCC-http://fofcc.org.cn/mn/11220/
When veterinary drugs leave the factory, a product quality inspection certificate must be attached; if there is no certificate, veterinary drug operating enterprises shall not deal in them.Өгүүлэл нь ...-аас авсанFOFCC-http://fofcc.org.cn/mn/11220/
Chapter III Administration of Veterinary Drug Operating EnterprisesӨгүүлэл нь ...-аас авсанFOFCC-http://fofcc.org.cn/mn/11220/
Article 11 Veterinary drug operating enterprises must meet the following conditions:Өгүүлэл нь ...-аас авсанFOFCC-http://fofcc.org.cn/mn/11220/
(1) Having veterinary drug technical personnel commensurate with the veterinary drugs to be operated;Өгүүлэл нь ...-аас авсанFOFCC-http://fofcc.org.cn/mn/11220/
(2) Having business premises, equipment and warehouse facilities commensurate with the veterinary drugs to be operated.Өгүүлэл нь ...-аас авсанFOFCC-http://fofcc.org.cn/mn/11220/
Article 12 To establish a veterinary drug operating enterprise, upon approval by the administrative department of animal husbandry and veterinary medicine of the local people's government at or above the county level, a Veterinary Drug Operating License shall be issued. A veterinary drug operating enterprise shall, with the Veterinary Drug Operating License, apply to the local administrative organ for industry and commerce for registration, and upon approval, obtain a Business License.Өгүүлэл нь ...-аас авсанFOFCC-http://fofcc.org.cn/mn/11220/
The Veterinary Drug Operating License shall specify a period of validity, and upon expiration, a new license shall be issued after re-examination and qualification.Өгүүлэл нь ...-аас авсанFOFCC-http://fofcc.org.cn/mn/11220/
Article 13 The purchase of veterinary drugs must undergo quality acceptance inspection. Those with unqualified quality shall not be purchased.Өгүүлэл нь ...-аас авсанFOFCC-http://fofcc.org.cn/mn/11220/
Article 14 The storage of veterinary drugs must establish and implement a warehousing and preservation system to ensure the quality and safety of veterinary drugs.Өгүүлэл нь ...-аас авсанFOFCC-http://fofcc.org.cn/mn/11220/
Article 15 The sale of veterinary drugs must ensure quality, verify accuracy, and correctly explain the action, use, method of administration, dosage and precautions of the veterinary drugs.Өгүүлэл нь ...-аас авсанFOFCC-http://fofcc.org.cn/mn/11220/
Article 16 Those operating veterinary drugs in urban and rural fair trade markets must hold a Veterinary Drug Operating License and a Business License.Өгүүлэл нь ...-аас авсанFOFCC-http://fofcc.org.cn/mn/11220/
Chapter IV Pharmaceutical Administration of Veterinary Medical UnitsӨгүүлэл нь ...-аас авсанFOFCC-http://fofcc.org.cn/mn/11220/
Article 17 Veterinary medical units must be equipped with veterinary drugs and veterinary technical personnel commensurate with their medical tasks, establish and improve a veterinary drug management system, and strengthen pharmaceutical administration.Өгүүлэл нь ...-аас авсанFOFCC-http://fofcc.org.cn/mn/11220/
Article 18 To prepare veterinary drug preparations, veterinary medical units must have facilities and inspection instruments that ensure the quality of the preparations, and upon examination and approval by the administrative department of animal husbandry and veterinary medicine of the people's government of the province, autonomous region or municipality directly under the Central Government where they are located, a Veterinary Drug Preparation License shall be issued.Өгүүлэл нь ...-аас авсанFOFCC-http://fofcc.org.cn/mn/11220/
The Veterinary Drug Preparation License shall specify a period of validity, and upon expiration, a new license shall be issued after re-examination and qualification.Өгүүлэл нь ...-аас авсанFOFCC-http://fofcc.org.cn/mn/11220/
Article 19 Veterinary drug preparations prepared by veterinary medical units must meet qualified standards before they may be used for clinical use by the unit itself and in the medical area under its responsibility, but shall not be sold on the market.Өгүүлэл нь ...-аас авсанFOFCC-http://fofcc.org.cn/mn/11220/
Article 20 When veterinary medical units purchase veterinary drugs, they must implement a quality acceptance inspection system, and unqualified ones shall not be used.Өгүүлэл нь ...-аас авсанFOFCC-http://fofcc.org.cn/mn/11220/
To facilitate the purchase of veterinary drugs by farmers and herdsmen, veterinary medical units may concurrently engage in the retail business of veterinary drugs.Өгүүлэл нь ...-аас авсанFOFCC-http://fofcc.org.cn/mn/11220/
Chapter V Approval of New Veterinary Drugs and Administration of Import and Export Veterinary DrugsӨгүүлэл нь ...-аас авсанFOFCC-http://fofcc.org.cn/mn/11220/
Article 21 The standards for veterinary drugs are divided into national standards, industry standards and local standards.Өгүүлэл нь ...-аас авсанFOFCC-http://fofcc.org.cn/mn/11220/
To produce veterinary drugs for which national standards, industry standards or local standards already exist, examination and approval by the administrative department of animal husbandry and veterinary medicine of the people's government of the province, autonomous region or municipality directly under the Central Government shall be required, and an approval number shall be issued.Өгүүлэл нь ...-аас авсанFOFCC-http://fofcc.org.cn/mn/11220/
Article 22 The State encourages the research and creation of new veterinary drugs.Өгүүлэл нь ...-аас авсанFOFCC-http://fofcc.org.cn/mn/11220/
To develop new veterinary drugs, relevant materials such as development methods, production processes, quality standards, pharmacology, toxicology, clinical trial reports, environmental impact reports and pollution prevention and control measures, as well as samples of the new veterinary drugs, must be submitted to the administrative department of animal husbandry and veterinary medicine under the State Council. After the new veterinary drugs are reviewed and appraised by the State veterinary drug supervisory institution and proven safe and effective, they shall be examined and approved by the administrative department of animal husbandry and veterinary medicine under the State Council, listed as national standards or industry standards, and a New Veterinary Drug Certificate shall be issued. Without a New Veterinary Drug Certificate, they shall not be listed as formal scientific research achievements or be subject to technology transfer.Өгүүлэл нь ...-аас авсанFOFCC-http://fofcc.org.cn/mn/11220/
Article 23 To develop new veterinary drug preparations, materials such as the formula and preparation process, quality standards and clinical trial reports of the new preparations must be submitted to the administrative department of animal husbandry and veterinary medicine of the people's government of the province, autonomous region or municipality directly under the Central Government where they are located. After review and appraisal by the veterinary drug supervisory institute of the province, autonomous region or municipality directly under the Central Government and proof of safety and efficacy, they shall be examined and approved by the administrative department of animal husbandry and veterinary medicine of the people's government of the province, autonomous region or municipality directly under the Central Government and listed as local standards.Өгүүлэл нь ...-аас авсанFOFCC-http://fofcc.org.cn/mn/11220/
Article 24 To produce new veterinary drugs and new veterinary drug preparations, they must pass inspection by the veterinary drug supervisory institute of the province, autonomous region or municipality directly under the Central Government, and upon approval by the administrative department of animal husbandry and veterinary medicine of the people's government of the province, autonomous region or municipality directly under the Central Government, an approval number shall be issued.Өгүүлэл нь ...-аас авсанFOFCC-http://fofcc.org.cn/mn/11220/
Article 25 For the import of veterinary drugs, examination and approval by the administrative department of animal husbandry and veterinary medicine under the State Council or the administrative department of animal husbandry and veterinary medicine of the people's government of the province, autonomous region or municipality directly under the Central Government shall be required, and an Import Veterinary Drug License shall be issued; import may be carried out only after inspection by the veterinary drug supervisory institute designated by the administrative department of animal husbandry and veterinary medicine of the people's government of the province, autonomous region or municipality directly under the Central Government or by the administrative department of animal husbandry and veterinary medicine under the State Council and qualification.Өгүүлэл нь ...-аас авсанFOFCC-http://fofcc.org.cn/mn/11220/
Article 26 When China imports for the first time a certain veterinary drug produced or operated by a foreign enterprise, the foreign enterprise selling the veterinary drug must also apply to the administrative department of animal husbandry and veterinary medicine under the State Council for inspection and registration, and provide materials such as the quality standards, inspection methods, pharmacological and toxicological test results, clinical trial reports and instructions for use of the veterinary drug, as well as documentary proof that the exporting country (region) has approved its production or sale. After inspection and review and proof of safety and efficacy, an Import Veterinary Drug Registration License shall be issued.Өгүүлэл нь ...-аас авсанFOFCC-http://fofcc.org.cn/mn/11220/
Article 27 The State shall implement protection for the undisclosed test data and other data obtained by the applicant itself and submitted for veterinary drugs containing new compounds that have been approved or registered in accordance with law.Өгүүлэл нь ...-аас авсанFOFCC-http://fofcc.org.cn/mn/11220/
Within 6 years from the date of approval or registration, if other applicants apply for approval or registration of veterinary drugs using the data specified in the preceding paragraph without the consent of the applicant that has obtained approval or registration, the approval or registration authority shall not approve or register them; except where other applicants submit data obtained by themselves.Өгүүлэл нь ...-аас авсанFOFCC-http://fofcc.org.cn/mn/11220/
Except under the following circumstances, the approval or registration authority shall not disclose the data specified in the first paragraph:Өгүүлэл нь ...-аас авсанFOFCC-http://fofcc.org.cn/mn/11220/
(1) The need for public interest;Өгүүлэл нь ...-аас авсанFOFCC-http://fofcc.org.cn/mn/11220/
(2) Measures have been taken to ensure that such information will not be improperly used for commercial purposes.Өгүүлэл нь ...-аас авсанFOFCC-http://fofcc.org.cn/mn/11220/
Article 28 Import and export of veterinary narcotic drugs and psychotropic drugs must be accompanied by an Import Permit or Export Permit issued by the health administrative department under the State Council.Өгүүлэл нь ...-аас авсанFOFCC-http://fofcc.org.cn/mn/11220/
Chapter VI Supervision of Veterinary DrugsӨгүүлэл нь ...-аас авсанFOFCC-http://fofcc.org.cn/mn/11220/
Article 29 Production and sale of counterfeit veterinary drugs is prohibited. Any of the following circumstances shall constitute a counterfeit veterinary drug:Өгүүлэл нь ...-аас авсанFOFCC-http://fofcc.org.cn/mn/11220/
(1) Passing off non-veterinary drugs as veterinary drugs;Өгүүлэл нь ...-аас авсанFOFCC-http://fofcc.org.cn/mn/11220/
(2) The types and names of the ingredients contained in the veterinary drug do not conform to national standards, industry standards, or local standards.Өгүүлэл нь ...-аас авсанFOFCC-http://fofcc.org.cn/mn/11220/
Production and sale of veterinary drugs under any of the following circumstances is prohibited:Өгүүлэл нь ...-аас авсанFOFCC-http://fofcc.org.cn/mn/11220/
(1) Those for which an approval number has not been obtained;Өгүүлэл нь ...-аас авсанFOFCC-http://fofcc.org.cn/mn/11220/
(2) Those explicitly prohibited from use by the administrative department of animal husbandry and veterinary medicine under the State Council.Өгүүлэл нь ...-аас авсанFOFCC-http://fofcc.org.cn/mn/11220/
Article 30 Production and sale of inferior veterinary drugs is prohibited. Veterinary drugs under any of the following circumstances are inferior veterinary drugs:Өгүүлэл нь ...-аас авсанFOFCC-http://fofcc.org.cn/mn/11220/
(1) The content of ingredients in the veterinary drug does not conform to the provisions of national standards, industry standards, or local standards;Өгүүлэл нь ...-аас авсанFOFCC-http://fofcc.org.cn/mn/11220/
(2) Those beyond the expiration date;Өгүүлэл нь ...-аас авсанFOFCC-http://fofcc.org.cn/mn/11220/
(3) Those that cannot be used as medicine due to deterioration;Өгүүлэл нь ...-аас авсанFOFCC-http://fofcc.org.cn/mn/11220/
(4) Those that cannot be used as medicine due to contamination;Өгүүлэл нь ...-аас авсанFOFCC-http://fofcc.org.cn/mn/11220/
(5) Other cases that do not conform to veterinary drug standards but do not constitute counterfeit veterinary drugs.Өгүүлэл нь ...-аас авсанFOFCC-http://fofcc.org.cn/mn/11220/
Article 31 The administrative departments of animal husbandry and veterinary medicine of people's governments at or above the county level shall exercise the authority of supervision and administration over veterinary drugs.Өгүүлэл нь ...-аас авсанFOFCC-http://fofcc.org.cn/mn/11220/
The veterinary drug supervisory and inspection institutions of the State and of provinces, autonomous regions, and municipalities directly under the Central Government, as well as urban veterinary drug supervisory and inspection institutions established with the approval of the people's governments of provinces, autonomous regions, and municipalities directly under the Central Government, shall assist the administrative departments of animal husbandry and veterinary medicine and shall be respectively responsible for the quality supervision and inspection of veterinary drugs nationwide and within their respective jurisdictions.Өгүүлэл нь ...-аас авсанFOFCC-http://fofcc.org.cn/mn/11220/
Article 32 The administrative departments of animal husbandry and veterinary medicine at all levels shall regularly organize investigations, verification, and review of veterinary drugs that have been approved for production. For those with uncertain efficacy or that cannot guarantee medication safety, they shall, in accordance with their functions and powers, revoke their approval numbers. Veterinary drugs whose approval numbers have been revoked shall not continue to be produced or sold.Өгүүлэл нь ...-аас авсанFOFCC-http://fofcc.org.cn/mn/11220/
Article 33 The administrative departments of animal husbandry and veterinary medicine of people's governments at or above the county level shall appoint veterinary drug supervisors. Veterinary drug supervisors must be held by veterinary drug or veterinary technical personnel and shall carry out their work on the strength of the Veterinary Drug Supervisor Certificate issued by the people's government to which they belong.Өгүүлэл нь ...-аас авсанFOFCC-http://fofcc.org.cn/mn/11220/
Veterinary drug supervisors have the right, in accordance with the provisions of these Regulations, to supervise and inspect the quality of veterinary drugs in units producing, selling, and using veterinary drugs within their jurisdictions, and when necessary may, in accordance with regulations, take samples and obtain necessary materials; the units concerned shall not refuse or conceal information. Veterinary drug supervisors shall have the obligation to keep confidential the technical materials provided by veterinary drug production and scientific research units.Өгүүлэл нь ...-аас авсанFOFCC-http://fofcc.org.cn/mn/11220/
Article 34 Veterinary drug production enterprises, veterinary drug selling enterprises, and veterinary medical units shall frequently inspect the quality, efficacy, and safety of the veterinary drugs they produce, sell, and use.Өгүүлэл нь ...-аас авсанFOFCC-http://fofcc.org.cn/mn/11220/
When a veterinary drug user discovers a veterinary drug poisoning accident, it must promptly report it to the local administrative department of animal husbandry and veterinary medicine.Өгүүлэл нь ...-аас авсанFOFCC-http://fofcc.org.cn/mn/11220/
Article 35 The veterinary drug inspection institutions or personnel of veterinary drug production enterprises and veterinary drug selling enterprises shall receive professional guidance from the local veterinary drug supervisory and inspection institute.Өгүүлэл нь ...-аас авсанFOFCC-http://fofcc.org.cn/mn/11220/
Article 36 Special drugs such as veterinary narcotic drugs, psychotropic drugs, toxic drugs, and radioactive drugs shall be managed in accordance with relevant state provisions.Өгүүлэл нь ...-аас авсанFOFCC-http://fofcc.org.cn/mn/11220/
Article 37 Units and individuals using veterinary drugs shall comply with the safe use provisions for veterinary drugs formulated by the administrative department of animal husbandry and veterinary medicine under the State Council. It is prohibited to use counterfeit veterinary drugs, inferior veterinary drugs, veterinary drugs whose production and sale are prohibited under paragraph 2 of Article 29 of these Regulations, and veterinary drugs imported without approval.Өгүүлэл нь ...-аас авсанFOFCC-http://fofcc.org.cn/mn/11220/
The administrative departments of animal husbandry and veterinary medicine of people's governments at or above the county level shall strengthen the detection of veterinary drug residues in animal products and shall publish the detection results. The residue limit standards and detection methods for veterinary drugs shall be formulated by the administrative department of animal husbandry and veterinary medicine under the State Council.Өгүүлэл нь ...-аас авсанFOFCC-http://fofcc.org.cn/mn/11220/
Chapter VII Management of Trademarks and Advertisements for Veterinary DrugsӨгүүлэл нь ...-аас авсанFOFCC-http://fofcc.org.cn/mn/11220/
Article 38 Veterinary drug trademarks shall be registered in accordance with the provisions of the state's trademark laws and regulations.Өгүүлэл нь ...-аас авсанFOFCC-http://fofcc.org.cn/mn/11220/
Registered trademarks must be indicated on the packaging, labels, and instructions of veterinary drugs, and the words “Registered Trademark” or a registration mark shall be noted.Өгүүлэл нь ...-аас авсанFOFCC-http://fofcc.org.cn/mn/11220/
Article 39 Veterinary drug advertisements must be examined and approved by the administrative department of animal husbandry and veterinary medicine under the State Council or the administrative department of animal husbandry and veterinary medicine of the people's government of a province, autonomous region, or municipality directly under the Central Government. Those not approved shall not be published, installed, printed, broadcast, distributed, or posted.Өгүүлэл нь ...-аас авсанFOFCC-http://fofcc.org.cn/mn/11220/
Article 40 The content of veterinary drug advertisements must be based on the instructions approved by the administrative department of animal husbandry and veterinary medicine under the State Council or the administrative department of animal husbandry and veterinary medicine of the people's government of a province, autonomous region, or municipality directly under the Central Government.Өгүүлэл нь ...-аас авсанFOFCC-http://fofcc.org.cn/mn/11220/
Veterinary narcotic drugs and psychotropic drugs shall not be advertised.Өгүүлэл нь ...-аас авсанFOFCC-http://fofcc.org.cn/mn/11220/
Article 41 Foreign enterprises applying in China to handle veterinary drug advertisements must hold an Import Veterinary Drug Registration Permit issued by the administrative department of animal husbandry and veterinary medicine under the State Council and shall provide veterinary drug instructions.Өгүүлэл нь ...-аас авсанFOFCC-http://fofcc.org.cn/mn/11220/
Chapter VIII Penalty ProvisionsӨгүүлэл нь ...-аас авсанFOFCC-http://fofcc.org.cn/mn/11220/
Article 42 For production or sale of counterfeit veterinary drugs or violation of the provisions of paragraph 2 of Article 29 of these Regulations, criminal liability shall be pursued in accordance with the provisions of the Criminal Law on the crime of producing or selling fake or inferior products or the crime of producing or selling fake or inferior veterinary drugs; if the case is not serious enough for criminal punishment, the party shall be ordered to stop producing or selling the veterinary drug, the drugs and illegal gains shall be confiscated, and a fine of not less than 1 time but not more than 5 times the illegal gains shall be imposed; and the enterprise may be ordered to suspend production, suspend business for rectification, or have its Veterinary Drug Production Permit, Veterinary Drug Selling Permit, or Veterinary Drug Preparation Permit revoked.Өгүүлэл нь ...-аас авсанFOFCC-http://fofcc.org.cn/mn/11220/
Article 43 For production or sale of inferior veterinary drugs, criminal liability shall be pursued in accordance with the provisions of the Criminal Law on the crime of producing or selling fake or inferior products or the crime of producing or selling fake or inferior veterinary drugs; if the case is not serious enough for criminal punishment, the party shall be ordered to stop producing or selling the veterinary drug, the drugs and illegal gains shall be confiscated, and a fine of not less than 1 time but not more than 5 times the illegal gains shall be imposed; if the circumstances and consequences are serious, the enterprise may also be ordered to suspend production, suspend business for rectification, or have its Veterinary Drug Production Permit, Veterinary Drug Selling Permit, or Veterinary Drug Preparation Permit revoked.Өгүүлэл нь ...-аас авсанFOFCC-http://fofcc.org.cn/mn/11220/
Article 44 Those who, without obtaining the Veterinary Drug Production Permit, Veterinary Drug Selling Permit, or Veterinary Drug Preparation Permit, produce or sell veterinary drugs or prepare veterinary drug preparations without authorization shall be pursued for criminal liability in accordance with the provisions of the Criminal Law on the crime of illegal business operations; if the case is not serious enough for criminal punishment, they shall be ordered to stop production, stop business, or stop preparing veterinary drug preparations, all veterinary drugs and illegal gains shall be confiscated, and a fine of not less than 1 time but not more than 5 times the illegal gains may also be imposed.Өгүүлэл нь ...-аас авсанFOFCC-http://fofcc.org.cn/mn/11220/
Article 45 Those who violate the provisions of these Regulations concerning the import of veterinary drugs shall be pursued for criminal liability in accordance with the provisions of the Criminal Law on the crime of illegal business operations; if the case is not serious enough for criminal punishment, a warning shall be given or the veterinary drugs shall be confiscated according to the seriousness of the circumstances; if they are sold without authorization, the illegal gains shall be confiscated, and a fine of not less than 1 time but not more than 5 times the illegal gains shall be imposed.Өгүүлэл нь ...-аас авсанFOFCC-http://fofcc.org.cn/mn/11220/
Article 46 Those who use veterinary drugs without complying with the relevant state provisions on safe use of veterinary drugs shall be given a warning and may also be fined not more than 30,000 yuan.Өгүүлэл нь ...-аас авсанFOFCC-http://fofcc.org.cn/mn/11220/
Those who use counterfeit veterinary drugs, inferior veterinary drugs, or other veterinary drugs prohibited from use shall be ordered to stop using them, the drugs shall be confiscated, and a fine of not less than 10,000 yuan but not more than 50,000 yuan may also be imposed.Өгүүлэл нь ...-аас авсанFOFCC-http://fofcc.org.cn/mn/11220/
Article 47 The administrative penalties provided for in these Regulations shall be decided by the administrative departments of animal husbandry and veterinary medicine of people's governments at or above the county level. However, where administrative penalties should be imposed for violation of Article 16 and Chapter VII of these Regulations; where illegal gains should be confiscated and fines imposed in accordance with Article 45 of these Regulations; and where illegal gains should be confiscated and fines imposed for violation of the relevant provisions of the Regulations on Quality Responsibility for Industrial Products in the production or sale of veterinary drugs, the decision shall be made by the administrative authorities for industry and commerce, with the administrative departments of animal husbandry and veterinary medicine assisting in investigation and handling.Өгүүлэл нь ...-аас авсанFOFCC-http://fofcc.org.cn/mn/11220/
Fines and confiscated illegal gains shall all be turned over to the state treasury. Confiscated counterfeit and inferior drugs and other drugs explicitly prohibited from use by the state shall be destroyed by the administrative departments of animal husbandry and veterinary medicine.Өгүүлэл нь ...-аас авсанFOFCC-http://fofcc.org.cn/mn/11220/
Article 48 If a party is dissatisfied with a decision on administrative penalty, it may bring a suit in a people's court within 15 days from the date of receiving notice of the penalty decision. However, the party must execute decisions made by the administrative departments of animal husbandry and veterinary medicine concerning veterinary drug control. If a penalty decision is not performed and no suit is brought after the time limit expires, the organ that made the administrative penalty decision shall apply to a people's court for compulsory enforcement.Өгүүлэл нь ...-аас авсанFOFCC-http://fofcc.org.cn/mn/11220/
Article 49 If violation of the provisions of these Regulations causes a poisoning accident or other harmful consequences to livestock, poultry, or other animals, the unit or individual causing the harm shall bear liability for compensation. The injured party may request the administrative department of animal husbandry and veterinary medicine of a people's government at or above the county level to handle the matter. If a party is dissatisfied with the handling decision, it may bring a suit in a people's court within 15 days from the date of receiving notice.Өгүүлэл нь ...-аас авсанFOFCC-http://fofcc.org.cn/mn/11220/
The injured party may also bring a suit directly in a people's court.Өгүүлэл нь ...-аас авсанFOFCC-http://fofcc.org.cn/mn/11220/
A claim for compensation shall be raised within 1 year from the date on which the injured party knew or should have known that its rights were infringed; if the time limit is exceeded, it shall not be accepted.Өгүүлэл нь ...-аас авсанFOFCC-http://fofcc.org.cn/mn/11220/
Chapter IX Supplementary ProvisionsӨгүүлэл нь ...-аас авсанFOFCC-http://fofcc.org.cn/mn/11220/
Article 50 The meanings of the following terms in these Regulations are:Өгүүлэл нь ...-аас авсанFOFCC-http://fofcc.org.cn/mn/11220/
(1) Livestock, poultry, and other animals: refers to domestic animals, poultry, fish, bees, silkworms, and other artificially raised animals.Өгүүлэл нь ...-аас авсанFOFCC-http://fofcc.org.cn/mn/11220/
(2) Veterinary drugs: refers to substances used for the prevention, treatment, and diagnosis of diseases of livestock, poultry, and other animals, and for the purposeful regulation of their physiological functions, with specified actions, uses, methods of use, and dosage (including feed drug additives). These include:Өгүүлэл нь ...-аас авсанFOFCC-http://fofcc.org.cn/mn/11220/
1. Biological products such as sera, bacterial (vaccine) preparations, and diagnostic fluids;Өгүүлэл нь ...-аас авсанFOFCC-http://fofcc.org.cn/mn/11220/
2. Traditional Chinese medicinal materials, traditional Chinese patent medicines, chemical active pharmaceutical ingredients and their preparations for veterinary use;Өгүүлэл нь ...-аас авсанFOFCC-http://fofcc.org.cn/mn/11220/
3. Antibiotics, biochemical drugs, and radioactive drugs.Өгүүлэл нь ...-аас авсанFOFCC-http://fofcc.org.cn/mn/11220/
(3) New veterinary drugs: refers to newly developed veterinary active pharmaceutical ingredients in China.Өгүүлэл нь ...-аас авсанFOFCC-http://fofcc.org.cn/mn/11220/
(4) New veterinary drug preparations: refers to veterinary drug preparations newly developed and processed from veterinary active pharmaceutical ingredients.Өгүүлэл нь ...-аас авсанFOFCC-http://fofcc.org.cn/mn/11220/
Article 51 These Regulations shall come into force on January 1, 1988, and the Interim Regulations on Veterinary Drug Administration, approved and transmitted by the State Council on August 26, 1980, shall be repealed simultaneously.Өгүүлэл нь ...-аас авсанFOFCC-http://fofcc.org.cn/mn/11220/