What are the procedures for dealing in veterinary drugs?

Question 1: What are the procedures for selling veterinary drugs? 2. The issuance of veterinary drug production licenses, veterinary drug business licenses and veterinary drug preparation licenses must comply with the Regulations on the Administration of Veterinary Drugs, the Detailed Rules for the Implementation of the Regulations on the Administration of Veterinary Drugs and the provisions of these Measures. 3. Basic conditions for veterinary drug production enterprises. The personnel of a veterinary drug production enterprise must meet the following basic conditions: (1) The factory director must have a technical secondary school education or the corresponding technical title, be familiar with veterinary drug production technology and have been engaged in veterinary drug production for more than three years. (two) the person in charge of the department of veterinary drug production and quality inspection must be a professional and technical personnel with the titles of pharmacist, engineer and veterinarian, and engaged in veterinary drug production or inspection for more than three years. Quality inspection personnel should be technical personnel above technical secondary school or specially trained qualified inspectors. (3) Workers in veterinary drug production posts shall have a junior high school education or above, and quality inspection workers shall have a senior high school education or above, and be skilled in production and inspection operations after professional and technical training. Electricians, boiler workers and other auxiliary workers must pass the examination of the labor department. 4. The factory buildings and workshops of veterinary drug production enterprises must meet the following basic conditions: (1) There must be a clean environment, fire safety facilities and three wastes treatment facilities, and the production area and living area should be separated. Biological products factory should also have facilities to prevent the spread of drugs. If a non-veterinary drug factory concurrently engages in veterinary drugs, it must have a separate veterinary drug production area or workshop. (two) the layout of the factory and workshop should meet the requirements of production technology, and there should be enough space and place to arrange equipment and pile up materials neatly and reasonably. All procedures of drugs of different varieties and specifications shall not be operated in the same room. The main production workshops should have dust-proof, bacteria-proof, mosquito-proof and insect-proof facilities, especially the refining, drying and packaging workshops and preparation workshops of raw materials. (three) the production of sterile preparations, the workshop should have air purification device, sterile buffer room and closed and isolated studio. The production of Chinese patent medicine should have a drying field. Biological products production should also have aseptic operation room, animal feeding room, corpse incineration facilities and sewage treatment equipment. (four) the veterinary drug factory should have storage facilities suitable for the production of veterinary drugs. Raw materials, auxiliary materials, intermediates, semi-finished products, finished products and unqualified products must be stored separately and clearly marked. Drugs with special requirements must have adequate storage conditions. Other items shall not be stored in the cold storage of biological products at the same time. 5. According to the varieties produced, veterinary drug production enterprises should have the following basic drug production equipment: (1) water injection: heavy distilled water, stainless steel mixing tank, film filter, round knife, bottle washer, ampoule dryer, autoclave, printing and packaging machine, air filtration and ventilation equipment, etc. (2) Powder injection: there should be bottle washing machine, bottle drying equipment, metering and subpackaging device, capping machine, etc. (3) Tablets: there should be pulverizer, mixer, granulator, tablet press, drying equipment and air dust removal equipment. (4) Feed drug additives: there should be pulverizers, electric sieves, dryers, twin-screw mixers and metering and dispensing machines. Drugs that are easy to oxidize and fail should be packed by vacuum nitrogen filling packaging machine. (5) Chinese medicinal powder: there should be pulverizer, mixer, electric sieve, medicine washing pool, dust-proof and drying equipment, etc. (6) Biological products: there should be bottle spinners, culture tanks, filters, freeze dryers, incubators, capping packaging machines, autoclaves, ovens, refrigeration equipment, etc. 6 quality inspection institutions of veterinary drug production enterprises must comply with the provisions of Article 7 of the Detailed Rules for the Implementation of the Regulations on the Administration of Veterinary Drugs. Quality inspection institutions are directly under the leadership of the factory director. Quality inspection institutions should have strict sampling, inspection records and inspection report audit system, and formulate quality inspection procedures. 7. Veterinary drug production enterprises should establish necessary systems: inspection and use system of raw and auxiliary materials, inspection system of semi-finished products, examination and approval system of new products, handling system of major quality accidents, safety system, hygiene system, personal hygiene physical examination system, etc. There should be production technology and operating procedures. 8 raw materials, auxiliary materials, containers, packaging materials, packaging, labels and products used by veterinary drug production enterprises shall comply with the provisions of the Regulations on the Administration of Veterinary Drugs and its detailed rules for implementation. Basic conditions for a veterinary drug trading enterprise Article 10 The personnel of a veterinary drug trading enterprise must comply with the provisions of Article 16 of the Detailed Rules for the Implementation of the Regulations on the Administration of Veterinary Drugs. Eleventh veterinary drug enterprises must have business offices, warehouses, shelves, storage places, counters and so on. There is a place suitable for its business, and drugs may not be stored in the open air. Twelfth business premises and warehouses should be clean and tidy, and there are fire safety facilities. The stacking, storage and arrangement of drugs should be neat. Article 13 ... >>

Question 2: What documents and procedures do you need to open a veterinary drug store? Just get a veterinary drug business license!

First, hire a veterinary pharmacist qualification certificate and certificate to apply for a business license in the drug supervision department, and then register with the local industrial and commercial bureau to obtain a business license.

The following are the ways to apply for a business license:

Notice of approval of veterinary drug management project

1. Approval basis: Regulations on the Administration of Veterinary Drugs in People's Republic of China (PRC) and Detailed Rules for the Implementation of Regulations on the Administration of Veterinary Drugs in People's Republic of China (PRC).

Second, the examination and approval criteria:

1, veterinary drug business enterprises engaged in the procurement, storage, sale, dispensing and inspection of veterinary drugs shall be pharmacists, veterinary technicians and above. Non-pharmaceutical and veterinary technicians must pass the examination of veterinary drug management knowledge.

2, veterinary drug business enterprises to buy, keep and sell veterinary drugs, must establish and improve the quality acceptance and warehousing acceptance, warehousing inspection, warehousing inspection, sales inspection system. Veterinary drug enterprises must accept the purchase of veterinary drugs. The contents of inspection and acceptance include: veterinary drug name, specification, manufacturer, production batch number, expiration date, approval number, production license number, veterinary drug mark, generic product name, active ingredients, drug withdrawal period, inspection certificate, packaging and appearance quality, etc.

3, veterinary drug business enterprises have business offices, warehouses, shelves, counters, veterinary drug storage and storage places must conform to the physical and chemical properties of all kinds of drugs. There are facilities such as pollution prevention, moth prevention, rat prevention, dust prevention, moisture prevention and mildew prevention. Drugs that need to be kept away from light and at low temperature have special equipment. There are fire safety facilities. The business premises and warehouses shall be clean and tidy, and the drugs shall be stacked, stored and displayed in a neat manner. Drugs shall not be stored in the open air.

4. There are standardized measuring instruments, clean and non-toxic sales tools and packaging materials.

5, in line with other conditions stipulated by the state, province and city.

Three. Materials submitted for approval:

1, bid for a written report;

2, "veterinary drug business license" application registration form;

3. A copy of the legal representative's ID card or temporary residence permit;

4. A copy of the ID card or temporary residence permit, academic certificate and professional title certificate of the pharmacist or veterinary technician;

5, the legal representative, staff veterinary drug business legal training examination certificate;

6. Employee employment contract and its copy;

7, business premises and warehouse housing ownership certificate or lease agreement;

8. Location and internal layout of business premises and warehouses;

9. List of facilities and photos;

10, management system list and data;

Four. Examination and approval procedures:

1. After accepting the application, the agricultural administrative department of each district and county (city) shall complete the examination and approval within five working days. If the examination and approval considers it necessary to improve the conditions, in accordance with the provisions of the notification commitment system, a notification commitment letter for the examination and approval of veterinary drug management projects will be issued, and the veterinary drug business license will be issued after being signed by the applicant to ensure that the conditions for examination and approval are met according to the regulations;

2, the district and county (city) administrative department of agriculture will, within one month from the date of issuing the certificate, notify the enterprises (individual industrial and commercial households) that have obtained the certificate by way of commitment, and conduct on-the-spot inspection on whether they meet the examination and approval conditions.

Verb (abbreviation of verb) Approval department and contact information:

The name, address, telephone number and postal code of the agricultural department of each district and county (city) (omitted)

Six, after opening shall meet the following requirements:

Veterinary drug management regulations and detailed rules for the implementation of veterinary drug management regulations

Question 3: What are the requirements for opening a veterinary drug store? Basic conditions and specific steps for opening a veterinary drug store.

1, veterinary drugs should meet the following conditions:

(1) Veterinary drug technicians who are suitable for the veterinary drugs they operate.

(2) Having business premises, equipment and warehouses suitable for the veterinary drugs it deals in.

(3) A quality management organization or personnel suitable for the veterinary drugs it deals in.

(four) other operating conditions stipulated in the quality management standards for veterinary drugs. In line with the above conditions, the applicant may apply to the veterinary administrative department of the people's government of the city or county, and attach the supporting materials.

(5) To start a veterinary drug store, you need to apply for a veterinary drug business license, an industrial and commercial business license, a tax registration certificate and a GSP acceptance certificate.

Among them, the acceptance of veterinary drug GSP includes veterinary qualification certificate, which requires a veterinary college diploma or above to qualify for the exam. It doesn't matter if there is no one. You can pay someone with this certificate from the local animal husbandry bureau to be your technical consultant. In other words, if you don't have this veterinary qualification certificate, you must ask someone with this qualification certificate to be your technical consultant. Otherwise, you have no legal right to write a prescription.

2. What are the steps to open a veterinary drug store?

Your first step is to apply for a veterinary drug business license at the local animal husbandry bureau, and he will tell you how to do it. Then go to the local administration for industry and commerce for business license, and then go to the local tax bureau for tax registration certificate. Then you can start a business.

(1) Approval conditions:

A having veterinary drug technicians who are suitable for the veterinary drugs they operate. (Personnel requirements: Personnel engaged in animal diagnosis and treatment activities in rural areas should have a technical secondary school education or equivalent veterinary professional education or have been engaged in veterinary work in rural areas for more than three years, and have obtained the qualification certificate of animal prevention and control personnel stipulated by the state or province, or have obtained the qualification of assistant veterinarian or above. Those who engage in diagnosis and treatment activities in towns at or above the county level have higher requirements. )

(2) It has business premises, equipment and storage facilities suitable for the veterinary drugs it deals in.

(2) Examination and approval procedures: the unit or individual shall report to the Municipal Animal Husbandry Center (Animal Husbandry Squadron) and issue a veterinary drug business license after examination and approval by the Municipal Agriculture and Forestry Bureau.

(3) Approval time: within one month after receiving all materials or within 7 days of commitment.

(4) Cost: 50 yuan/certificate.

Question 4: What documents does an individual need to open a veterinary drug store? First, the basis for handling

Company Law of People's Republic of China (PRC) and Regulations of the People's Republic of China on the Administration of Company Registration.

Second, handle the materials that need to be submitted

1. Application for company establishment registration signed by the legal representative of the company;

2. The certificate of designated representative or entrusted agent signed by all shareholders and a copy of the identity certificate of designated representative or entrusted agent;

The handling matters, authority and authorization period of the designated representative or entrusted agent shall be indicated.

3. Articles of Association signed by all shareholders;

4. Copy of shareholder qualification certificate or identity certificate of natural person;

If the shareholder is an enterprise, a copy of the business license shall be submitted; If the shareholder is an enterprise legal person, a copy of the registration certificate of the enterprise legal person shall be submitted; If the shareholder is an enterprise legal person, a copy of the registration certificate of the enterprise legal person shall be submitted; If the shareholder is a private non-enterprise unit, a copy of the certificate of the private non-enterprise unit shall be submitted; If the shareholder is a natural person, submit a copy of the identity certificate; Other shareholders shall submit qualification certificates stipulated by relevant laws and regulations.

5. A capital verification certificate issued by a legally established capital verification institution;

6. If the shareholder's capital contribution for the first time is non-monetary property, submit the certification documents that have gone through the formalities of property right transfer;

7. Copies of appointment documents and identity documents of directors, supervisors and managers;

Submit resolutions of the shareholders' meeting, resolutions of the board of directors or other relevant materials in accordance with the Company Law and the Articles of Association. The resolutions of the shareholders' meeting shall be signed by the shareholders, and the resolutions of the board of directors shall be signed by the directors.

8 copies of the legal representative's post-holding documents and identity documents;

9, proof of residence use;

Submit a copy of the property ownership certificate of the own property; A copy of the lease agreement and the lessor's property right certificate shall be submitted for the leased house. If the house is an urban house without obtaining the property right certificate, submit the certificate of the real estate management department or the certificate of completion acceptance, a copy of the purchase contract and the house sales license; Non-urban housing, submit the relevant proof of local regulations. If the lessor is a hotel or restaurant, it shall submit a copy of the business license of the hotel or restaurant. If a general uses real estate as a residence, he shall submit a copy of the military real estate lease license.

If the house is changed into a business house, if it is an urban house, it shall also submit the registration schedule-the registration form of residence (business premises) and the certificate issued by the local residents' committee (or owners' committee) that the interested owners agree to change the house into a business house; Non-urban housing, submit the relevant proof of local regulations.

10, notice of pre-approval of enterprise name;

1 1. If laws, administrative regulations and decisions of the State Council require approval for the establishment of a limited liability company, submit a copy of the relevant approval documents or license certificate;

12. If there are veterinary drug production projects in the business scope of the company's application for registration, submit a copy of the veterinary drug production license issued by the provincial animal husbandry and veterinary administrative bureau; If there is a veterinary drug business project, a copy of the veterinary drug business license issued by the Municipal Bureau of Agriculture shall be submitted.

note:

1. The application form and other application materials submitted shall be A4 paper.

2, the above did not indicate the copy, should be submitted to the original; Where a copy is submitted, it shall be marked "consistent with the original" and signed by the shareholders, or the designated representative or entrusted agent shall affix the official seal or sign.

3. If the above involves the signature of shareholders, the natural person shareholder shall sign by himself; Shareholders other than natural persons affix their official seals.

4, according to the statutory conditions and procedures, need to verify the substance of the application materials, according to the law to verify.

Third, the handling procedures

Application-Acceptance-Examination-Decision

Fourth, the processing cycle.

If the application materials are complete and conform to the statutory form, the business license shall be obtained within three working days from the date of receiving the acceptance notice.

Verb (abbreviation for verb) cost

Free ... >>

Question 5: What documents do I need to open a veterinary drug store? Conditions for obtaining a business license for veterinary drugs:

(1) It has veterinary technicians and qualities suitable for the veterinary drugs it deals in.

Responsible person. Veterinary drug technicians must have a technical secondary school degree or above in related majors; The person in charge of quality should be a veterinary technician or above, or a junior professional title or a veterinary technical secondary school education or above, and not in other units.

(2) Having business premises, warehouses and goods suitable for the operation of veterinary drugs and business.

Shelves, counters and other facilities are not allowed to store veterinary drugs in the open air. Business offices and warehouses should be set up separately, and the comprehensive area of business offices and warehouses should not be less than 40 square meters (county) or 30 square meters (rural).

(3) The operation room and warehouse should be clean and tidy, with anti-pollution and insect-proof bars.

Rat-proof, fire-proof, moisture-proof and mildew-proof facilities and drugs with special requirements shall be implemented in accordance with relevant regulations.

(4) Having a quality management organization or personnel suitable for the veterinary drugs it deals in. Establish and improve the ledger of veterinary drug purchase, storage and sales, and strictly implement quality management systems such as warehousing acceptance, warehousing custody, outbound inspection and distribution, and sales registration.

(5) Having other business conditions for veterinary drugs as stipulated by the state.

In line with the conditions specified in the preceding paragraph, the applicant may apply to the veterinary administrative department of the people's Republic of China at the county level, and attach the certification materials that meet the conditions specified in the preceding paragraph.

The veterinary administrative department of the local people's government at or above the county level shall complete the examination within 30 working days from the date of accepting the application. Those who pass the examination shall be issued a business license for veterinary drugs; Unqualified, it shall notify the applicant in writing. The applicant shall go through the industrial and commercial registration formalities with the veterinary drug business license.

Question 6: What documents do I need to open a veterinary drug store? Conditions for opening a veterinary drug store: the veterinary drug store has passed GSP certification, obtained a veterinary drug business license, and obtained an industrial and commercial business license. The veterinary drug store has complete legal qualifications.

If you want to sell veterinary prescription drugs, you need someone who can prescribe them, that is, a licensed veterinarian.

Above.

Question 7: I want to open a veterinary medicine shop. What formalities do I need to go through? In fact, the state has never restricted individuals from running pharmacies. The operation of pharmacies was opened to individuals as early as 1998. At present, all provinces in China have pharmacies run by individuals. However, the policy tendency of individual investment in opening pharmacies varies greatly from place to place. You'd better consult the local drug supervision and administration institution. The investment in opening a pharmacy is relatively large. Take an 80-square-meter storefront as an example, the start-up capital should be 200,000-300,000 yuan. Individuals who invest in opening pharmacies should also consider the scale of operation according to their own funds.

According to the provisions of the Drug Administration Law, the establishment of a pharmaceutical trading enterprise must meet the following conditions: (1) having qualified pharmaceutical technicians according to law; (2) Having business premises, equipment, storage facilities and sanitary environment suitable for the drugs handled; (3) It has a quality management organization or personnel suitable for the drugs it deals in; (4) Having rules and regulations to ensure the quality of drugs.

To apply for the establishment of a pharmacy, an application shall be made to the local municipal drug regulatory agency or the county-level drug regulatory agency directly established by the drug regulatory department of the people's government of a province, autonomous region or municipality directly under the Central Government. The pharmaceutical supervisory and administrative institution that accepts the application shall, within 30 working days from the date of receiving the application, make a review in accordance with the provisions of the pharmaceutical supervisory and administrative department of the State Council, combined with the number, region, traffic conditions and actual needs of the local resident population, and make a decision on whether to approve the preparation.

After the establishment of the proposed enterprise is completed, the applicant shall apply to the original examination and approval authority for acceptance. The original examination and approval authority shall, within 30 working days from the date of receiving the application, organize the acceptance in accordance with the relevant provisions of the Drug Administration Law; Those who meet the requirements shall be issued with a Pharmaceutical Business License. The applicant shall register with the administrative department for industry and commerce according to law with the Pharmaceutical Business License.

The process of applying for starting a pharmaceutical wholesale enterprise is basically consistent with the above procedures.

In addition, the implementation regulations also stipulate that the validity period of the Drug Business License is five years. If it is necessary to continue to deal in drugs at the expiration of the validity period, the licensed enterprise shall apply for renewal of the Drug Business License six months before the expiration of the validity period of the license in accordance with the provisions of the drug supervision and administration department of the State Council. Where a pharmaceutical trading enterprise stops trading drugs or suspends business, the original issuing authority shall cancel the Pharmaceutical Trading License.

The examination and approval authority of the autonomous region: Autonomous Region Drug Administration; Place and time of acceptance: Market Supervision Department of Autonomous Region Drug Administration; Address: No.9 Xinmin Road, Urumqi; Tel: 099/kloc-099 1-2629949；; Supervision telephone number: 099/kloc-099 1-2660453；;

Specific application and submission materials:

1. The original, photocopy and resume of the academic credentials of the legal representative, the person in charge of the enterprise and the person in charge of quality of the bidding enterprise;

2. The original and photocopy of the practicing certificate of licensed pharmacist;

3. The scope of drugs to be handled;

4. Proposed business premises, equipment, storage facilities and surrounding sanitary environment.

The above materials are in duplicate, printed and bound on A4 paper (the same below).

The drug administration of the autonomous region shall, within 30 working days from the date of accepting the application, review the application materials according to the Standards for the Establishment of Drug Wholesale Enterprises, make a decision on whether to approve the preparation, and notify the applicant in writing.

After obtaining the approval document of the preparation and completing the preparation, the applicant shall submit an application for acceptance to the drug administration of the autonomous region and submit the following materials:

1, drug business license application form;

2, the approval document issued by the administrative department for Industry and commerce;

3, the organization of the proposed enterprise;

4, business premises, warehouse layout and housing property rights or use rights certificate;

5. Qualification certificates and letters of appointment of pharmaceutical technicians who have obtained qualifications according to law;

6 planning enterprise quality management documents and storage facilities and equipment directory.

After receiving the application for enterprise acceptance, the drug administration of the autonomous region shall, within 30 working days, organize on-site acceptance according to the Implementation Standards for Acceptance of Drug Wholesale Enterprises Established by the State Food and Drug Administration of the United States (for Trial Implementation), and make a conclusion of conformity or non-conformity. Do not meet the standards, issued a "notice of acceptance and rectification", the enterprise should complete the rectification within 30 days, put forward an application for review, and the drug administration of the autonomous region will organize another acceptance.

If it meets the standards after on-site acceptance, the drug administration of the autonomous region will publicize it to the public through the website of the drug administration of the autonomous region 10 day. After the expiration of the publicity period, if there is no objection, the drug administration of the autonomous region will issue the Drug Business License and make an announcement on the website of the drug administration of the autonomous region; Objection to be investigated ... >>

Question 8: What are the procedures for opening a veterinary drug store? Just get a veterinary drug business license! First, find a person with a professional veterinary qualification certificate, preferably a letter of employment, and then take the certificate to the drug supervision department to apply for a business license, and then register with the local industrial and commercial bureau to obtain a business license. Veterinary drugs can be prescribed. Please consult the local animal husbandry bureau. However, after opening a veterinary drug store, you have to pass a GSP certification.

Question 9: What materials do you need for a veterinary drug business license? Chuanliao 1 and the Application Form for Veterinary Drug Business License shall be submitted in triplicate.

2, the qualifications, professional titles, qualifications of veterinary practitioners and certification materials before veterinary practice;

3. Various management systems;

4. Copy of employee ID card and 3 one-inch bareheaded photos of the person in charge;

5, veterinary drug business premises, equipment and other materials;

6, safety and quality commitment. Application procedure: (1) The applicant submits a written application to the county-level animal health supervision institution.

(2) After receiving the application report, the animal health supervision institution at the county level shall send veterinary drug supervisors to conduct on-site inspection and evaluation. If the results meet the establishment requirements and the layout is reasonable, the Application Form for Veterinary Drug Business License will be issued.

(3) The applicant fills in the Application Form for Veterinary Drug Business License, goes through the signing formalities according to the requirements listed in the table, and submits it to the supervision unit for review.

(4) The supervision unit shall report to the Agriculture Bureau for examination and approval, and issue the business license of veterinary drugs within 60 working days in accordance with the Regulations on the Administration of Veterinary Drugs and the documents of the Ministry of State II and the National Bureau.

(5) The applicant shall apply to the industrial and commercial department for registration with the Veterinary Drug Business License and obtain the business license before operating.

(6) The validity period of the Veterinary Drug Business License is five years, and it is reviewed once a year. The certified unit (or individual) shall submit the application for annual inspection to the supervision unit before the following year 1 month 15. If the annual inspection is not carried out after the expiration, it shall be handled as unlicensed operation and its business qualification shall be cancelled. Units and individuals engaged in veterinary drug business shall submit a written application to the veterinary health supervision department for on-site inspection and assessment. Units and individuals engaged in veterinary drug business approved by Xi Agriculture Bureau fill in the application form and issue the Veterinary Drug Business License within 60 working days.

Question 10: What are the procedures for running a small and medium-sized veterinary drug processing factory?

Veterinary drug production license (generally handled by Agriculture and Animal Husbandry Bureau), veterinary drug production approval document (generally handled by Quality Supervision Bureau), safety production license (generally handled by Safety Supervision Bureau), business license (generally handled by Industrial and Commercial Bureau) and tax registration certificate (generally handled by State Taxation Bureau and Local Taxation Bureau). There are other certificates, which are generally notified by the industrial and commercial department at the time of issuing the business license.