Is the department in charge of retail pharmacies the Food and Drug Administration, the Industrial and Commercial Bureau or the Ministry of Commerce?

Retail pharmacies apply to the industrial and commercial departments for business licenses after obtaining the Drug Retail License, and then apply for tax registration certificates with the business licenses. The quality of drugs is managed by the Food and Drug Administration, and the industrial and commercial departments supervise business practices (such as cheating consumers) and selling goods with counterfeit registered trademarks. Drug advertisements are managed by industry and commerce and drug supervision departments respectively. It seems that the business department has no supervision function on drugs. In fact, in China, it is normal for an operator to be supervised by multiple departments according to the duties and functions entrusted by laws and regulations because of the overlapping functions of departments.

Extended data:

Application materials for handling the Pharmaceutical Business License:

1. Drug and Medical Device Business License Management System Enterprise Preparation Application Form;

2, the legal representative of the proposed enterprise, the person in charge of the enterprise's academic qualifications, professional qualifications or professional titles, the original copy and resume;

3 types and scope of drugs to be handled;

4. Information on the business premises, storage facilities and equipment to be established (with the geographical location map and floor plan of the registered address (indicating the area), and indicating the shortest distance from the drug retail enterprise); Geographical location map and floor plan of the proposed warehouse (indicating area, length, width and height);

5. To start a retail (chain) enterprise, copies of the Drug Business License and Business License of each store and relevant assets certificates shall also be submitted;

6. Apply for the self-assurance statement of the authenticity of the materials, and promise to bear legal responsibility for the falsehood of the materials; If you need to submit a floppy disk, promise to be responsible for the loss of data files caused by the virus;

7. Where the applicant is not the legal representative or the person in charge, the enterprise shall submit two copies of Power of Attorney;

8. Make a catalogue in the order of application materials.

Three certificates for retail pharmacies:

1. Three Certificates of Drug Business (including drug wholesale and retail companies and pharmacies): drug business license, business license and GSP certification.

2. Pharmaceutical production category (pharmaceutical production enterprise): three certificates: pharmaceutical production enterprise license, pharmaceutical trading enterprise license and business license. Three certificates are new: drug production license, business license and GMP certificate (commonly known as "two certificates and one photo").