(1) with the production of veterinary drugs appropriate engineers, veterinarians and technical positions above the technical staff and skilled workers;
(2) with the production of veterinary drugs appropriate plant, facilities and sanitation environment;
(3) with the national labor Safety and health standards of the facilities and conditions;
(4) with quality inspection agencies and full-time inspectors and the necessary equipment;
(5) non-specialized production of veterinary drugs and veterinary drug production enterprises, there must be a separate veterinary drug production area. Article VI to open a veterinary drug production enterprises, must be by the county people's government animal husbandry and veterinary administrative departments of the enterprise agreed to by the people's governments of provinces, autonomous regions and municipalities directly under the Central People's Government of animal husbandry and veterinary administrative departments for examination and approval, and issued a "veterinary drug production license". Veterinary drug manufacturers with "veterinary drug production license" to the local industrial and commercial administrative organs to apply for registration, after approval to receive "business license".
"Veterinary Drug Production License" shall provide a validity period, the expiration of the re-examination of the license issued after passing. Article Veterinary drug manufacturers must be in accordance with technical regulations for production, production records must be complete and accurate, the required raw materials, auxiliary materials and direct contact with the veterinary drug containers and packaging materials, must meet the requirements of medicinal use. Article 8 The package of veterinary drugs must be labeled with the words "for veterinary use" and accompanied by instructions. Label or instructions must indicate the trademark, the name of the veterinary drug, specifications, the name of the enterprise, the product batch number and approval number, the main ingredients of veterinary drugs, content, function, use, usage, dosage, expiration date and precautions. Article 9 Veterinary drugs must be dispensed with complete and accurate dispensing records, and the name, specification, enterprise name, product lot number, approval number, dispensing unit and dispensing lot number of the veterinary drugs should be indicated on the package, together with the instructions. Veterinary drugs with specified expiration date must be indicated with expiration date after being dispensed. Article X veterinary drugs must undergo quality inspection before leaving the factory, does not meet the quality standards shall not leave the factory.
Veterinary drugs must be accompanied by a certificate of quality inspection; no certificate of conformity, veterinary drug business enterprises shall not operate. Chapter III of the management of veterinary drug business enterprises Article XI of veterinary drug business enterprises must have the following conditions:
(a) with the veterinary drugs operated by veterinary technicians;
(b) with the veterinary drugs operated by the appropriate business premises, equipment, warehouse facilities. Article XII of veterinary drug business enterprises, by the local people's governments at or above the county level, animal husbandry and veterinary administrative departments for approval, issued by the "veterinary drug business license". Veterinary drug business enterprises with "veterinary drug business license" to the local administrative organs for industry and commerce to apply for registration, after approval to receive the "business license".
"Veterinary drug business license" shall provide a validity period, the expiration of the re-examination of the license issued after passing. Article XIII of the acquisition of veterinary drugs must be quality inspection. Unqualified quality, shall not be acquired. Article XIV storage of veterinary drugs must establish and implement the warehousing and storage system to ensure the quality and safety of veterinary drugs. Article XV of the sale of veterinary drugs must ensure the quality of the check, and can correctly explain the role of veterinary drugs, use, usage, dosage and precautions. Article XVI in the urban and rural bazaars and trade markets operating veterinary drugs, must hold a "veterinary drug business license" and "business license. Chapter IV Veterinary Medical Units of pharmaceutical management Article XVII of veterinary medical units must be equipped with veterinary medicine, veterinary technicians appropriate to their medical tasks, the establishment of a sound veterinary drug management system to strengthen the management of pharmaceuticals. Article XVIII of the veterinary medical unit preparation of veterinary drugs, must have to ensure the quality of the preparation of facilities, testing instruments, and by the people's governments of the provinces, autonomous regions and municipalities directly under the Central People's Government of Animal Husbandry and Veterinary Administration review and approval of the issuance of "veterinary drug preparation license".
"Veterinary drug preparation license" shall provide a validity period, the expiration of the re-examination of the license issued after passing. Article 19 of the veterinary medical units formulated veterinary drug preparations, must meet the qualification standards, before the unit for the clinical and medical areas responsible for the use, but shall not be sold in the market. Article 20 The veterinary medical units to purchase veterinary drugs, must implement the quality acceptance system, unqualified shall not be used.
For the convenience of farmers and herdsmen to purchase veterinary drugs, veterinary medical units can also operate retail business of veterinary drugs. Chapter V Approval of new veterinary drugs and import and export of veterinary drug management Article 21 The standards of veterinary drugs are divided into national standards, industry standards and local standards.
Production of national standards, industry standards or local standards of veterinary drugs, must be approved by the people's governments of provinces, autonomous regions and municipalities directly under the Central People's Government of Animal Husbandry and Veterinary Administration, and issued approval number. Article 22 The state encourages the research and creation of new veterinary drugs.
Development of new veterinary drugs, must be reported to the State Council animal husbandry and veterinary administrative departments to develop methods, production processes, quality standards, pharmacology, toxicology, clinical trial reports, reports on the environmental impact and pollution control measures and other relevant information and samples of new veterinary drugs. New veterinary drugs by the State Veterinary Drug Supervisory Organization for review, identification, proof of safety and efficacy, by the State Council animal husbandry and veterinary administrative departments for examination and approval, as a national standard or industry standard, issued by the "Certificate of New Veterinary Drugs". No "Certificate of New Veterinary Drugs" shall not be included in the official scientific research results or technology transfer.