A, production enterprises:

1, business license of enterprise as a legal person;

2. Pharmaceutical production license;

3.GMP (Good Manufacturing Practice).

4. People's Republic of China (PRC) organization code;

5. Tax registration certificate;

6. Annual tax return;

7, enterprise quality questionnaire;

8. Quality assurance agreement.

Second, the product materials:

7, product production approval (or drug registration certificate);

8, product inspection report (the latest provincial inspection, generally required within 2 years);

9, product price documents (medical insurance products need regional prices);

10, product patent certificate file (provided, if not omitted);

1 1, trademark file;

12, inspection report of each batch of products (ex-factory inspection, used for sampling inspection in the first camp);

13, the smallest product packaging box (sample);

14, copy of drug instructions;

15, general taxpayer identification record (optional);

16, Power of Attorney of Legal Person (Power of Attorney of Legal Person);

17, copy of ID card;

18, product production standard;

19, purchase and sale contract;

20. Examination and approval of internal and external packaging and instructions of products;

2 1, qualification certificates of the buyer and the seller.

Third, the first business information of pharmaceutical companies:

1, business license of enterprise as a legal person;

2. Drug business license

3. Tax registration certificate;

4. People's Republic of China (PRC) organization code;

5. GSP (Good Supply Practice);

6. Account opening permit;

7. Bank transfer account number (name of billing unit, taxpayer identification number, address, telephone number, bank, account number);

8, supplier quality assurance system questionnaire;

9. Quality Assurance Agreement.

Extended data:

According to the Drug Administration Law of People's Republic of China (PRC):

Article 14 The establishment of a pharmaceutical wholesale enterprise shall be approved by the pharmaceutical supervisory and administrative department of the people's government of the province, autonomous region or municipality directly under the Central Government where the enterprise is located, and a Pharmaceutical Business License shall be issued; The establishment of a pharmaceutical retail enterprise must be approved by the local pharmaceutical supervisory and administrative department at or above the county level where the enterprise is located, and a Pharmaceutical Business License shall be issued. No drug business license, no drug business.

The Drug Business License shall indicate the validity period and business scope, and shall be re-examined and issued upon expiration.

When the pharmaceutical supervisory and administrative department approves the establishment of a pharmaceutical trading enterprise, it shall not only meet the conditions stipulated in Article 15 of this Law, but also follow the principle of rational distribution and convenience for the people to purchase medicines.

Article 15 To establish a pharmaceutical trading enterprise, the following conditions must be met:

(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 the drugs handled. ?

Article 16 Pharmaceutical trading enterprises must deal in pharmaceuticals in accordance with the Standards for Quality Control of Pharmaceutical Trading formulated by the State Council Pharmaceutical Supervision and Administration Department in accordance with this Law. The pharmaceutical supervisory and administrative department shall, in accordance with the provisions, certify whether the pharmaceutical trading enterprises meet the requirements of the Quality Management Standards for Pharmaceutical Trading; Those who pass the certification will get the certification certificate.

The specific implementation measures and steps of the "Quality Management Standards for Pharmaceutical Trading" shall be formulated by the drug supervision and administration department of the State Council.

Article 17 When purchasing drugs, pharmaceutical trading enterprises must establish and implement the system of inspection and acceptance of incoming goods, and verify the marks such as drug certificate; Do not meet the requirements, shall not be purchased.

Article 18 pharmaceutical trading enterprises must have true and complete records of purchasing and selling drugs. The purchase and sale records must indicate the general name, dosage form, specification, batch number, validity period, production enterprise, purchase (sales) unit, purchase (sales) quantity, purchase and sale price, purchase (sales) date and other contents as stipulated by the drug supervision and administration department of the State Council.

Article 19 Drug trading enterprises must sell drugs accurately, and correctly explain the usage, dosage and precautions; The prescription must be checked, and the drugs listed in the prescription shall not be changed or replaced without authorization. Prescriptions with incompatibility or overdose should be refused to be prepared; When necessary, it can be prepared only after being corrected or re-signed by the prescriber.

When selling Chinese herbal medicines, pharmaceutical trading enterprises must indicate the place of origin.

Article 20 Pharmaceutical trading enterprises must formulate and implement a drug storage system, and take necessary measures such as cold storage, anti-freezing, moisture prevention, insect prevention and rat prevention to ensure the quality of drugs. The storage and distribution of drugs must implement the acceptance system.

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