First, the required conditions:

1. Prepare the ID card and address materials of the operator;

2. Go to the local industrial and commercial office for a business license. For individuals, go to the industrial and commercial office; For the company, go to the industrial and commercial office;

3. Apply for tax registration certificate. The conditions of every Chinese medicine shop are not uniform. Generally speaking, it is required to have a medical practitioner and obtain the corresponding license.

Second, the formalities:

1, go to the local industrial and commercial office to apply for the business license of individual industrial and commercial households;

2. Go to the local State Taxation Bureau for tax registration certificate;

3. Go to the local local tax bureau for tax registration certificate;

4. There must be at least one licensed pharmacist. If you need an exam, you can register at the Personnel Testing Center.

5. Verify the relevant information required for invoice application (including the applicant's name, tax number, business address, invoice name, invoice code, invoice number, invoicing limit, etc.). );

6. Apply for the Pharmaceutical Business License.

To sum up, prepare the ID card and address materials of the operator; Go to the local industrial and commercial office for a business license. Individuals want to go to the industrial and commercial office, and companies want to go to the industrial and commercial office. Apply for tax registration certificate.

Legal basis:

Article 5 of the Measures for the Administration of Drug Business License

The establishment of a drug retail enterprise shall meet the requirements of the number of local permanent residents, regions, traffic conditions and actual needs, conform to the principle of facilitating people to buy drugs, and meet the following requirements:

(1) It has rules and regulations to ensure the quality of the drugs it deals in;

(2) Having qualified pharmaceutical technicians according to law;

Pharmaceutical retail enterprises dealing in prescription drugs and Class A OTC drugs must be equipped with licensed pharmacists or other qualified pharmaceutical technicians according to law. The person in charge of quality should have more than one year (including one year) experience in quality management of drug business.

Pharmaceutical retail enterprises dealing in Class B over-the-counter drugs and those established in rural areas below the township level shall be equipped with business personnel in accordance with Article 15 of the Regulations for the Implementation of the Drug Administration Law, and licensed pharmacists if conditions permit. During the business hours of the enterprise, the above-mentioned personnel shall be on duty.

(3) The enterprise, its legal representative, the person in charge of the enterprise and the person in charge of quality do not have the circumstances stipulated in Articles 75 and 82 of the Drug Administration Law;

(4) Having business premises, equipment, storage facilities and sanitary environment suitable for the drugs handled. The establishment of retail pharmacies in supermarkets and other commercial enterprises must have independent areas;

(five) have the ability to meet the needs of local consumers, and can guarantee the 24-hour supply. The quantity of national essential drugs that pharmaceutical retail enterprises should possess shall be determined by the food and drug supervision and administration departments of all provinces, autonomous regions and municipalities directly under the Central Government in light of local specific conditions.

If the state has other provisions on dealing in narcotic drugs, psychotropic drugs, toxic drugs for medical use and biological products for prevention, those provisions shall prevail.

Article 9

The establishment of a pharmaceutical retail enterprise shall handle the Pharmaceutical Business License in accordance with the following procedures:

(1) The applicant submits an application for preparation to the food and drug supervision and administration department at the municipal level located in the district where the proposed enterprise is located or the food and drug supervision and administration department at the county level directly established by the food and drug supervision and administration department of a province, autonomous region or municipality directly under the Central Government, and submits the following materials:

1. The original and photocopy of the academic qualifications, professional qualifications or professional titles of the legal representative, person in charge of the enterprise and person in charge of quality, resumes, professional and technical personnel qualification certificates and letters of appointment of the proposed enterprise;

2. The scope of drugs to be handled;

3 business premises, storage facilities and equipment to be established.

(2) The food and drug supervision and administration department shall handle the application submitted by the applicant according to the following circumstances:

1. If the application matters do not fall within the authority of the department, it shall immediately make a decision of rejection, issue a notice of rejection, and inform the applicant to apply to the relevant food and drug supervision and administration department.

2. If there are errors in the application materials that can be corrected on the spot, the applicant shall be allowed to correct them on the spot.

3. If the application materials are incomplete or do not conform to the statutory form, the applicant shall issue a Notice of Supplementary Materials on the spot or within 5 days to inform all the contents that need to be supplemented at one time. Fails to inform, since the date of receipt of the application materials is accepted.

4. If the application matters fall within the scope of functions and powers of the department, the materials are complete and conform to the statutory form, or the applicant submits all the corrected materials as required, it shall issue a notice of acceptance to the applicant. The date indicated in the bid-winning notice is the bid-winning date.

(3) The food and drug supervision and administration department shall, within 30 working days from the date of accepting the application, review the application materials according to the provisions of Article 5 of these Measures, make a decision on whether to approve the preparation, and notify the applicant in writing. If the applicant disagrees with the preparation, it shall explain the reasons and inform the applicant of the right to apply for administrative reconsideration or bring an administrative lawsuit according to law.

(four) after the preparation is completed, the applicant shall submit an application for acceptance to the food and drug supervision and administration department that accepts the application, and submit the following materials:

1. Application Form for Drug Business License;

2. Business license of the enterprise;

3 business premises, warehouse layout and proof of property right or use right of the house;

4. Qualification certificates and letters of appointment of pharmaceutical professional and technical personnel who have obtained qualifications according to law;

5. Quality management documents and main facilities and equipment catalogue of the enterprise to be established.

(5) The food and drug supervision and administration department that accepts the application shall, within 15 working days from the date of receiving the application, organize the acceptance according to the Implementation Standards for Accepting the Establishment of Pharmaceutical Retail Enterprises, and make a decision on whether to issue the Pharmaceutical Business License. If it does not meet the requirements, it shall notify the applicant in writing and explain the reasons. At the same time, the applicant shall be informed of the right to apply for administrative reconsideration or bring an administrative lawsuit according to law.