1 thought on “How to handle a drug business license”
Shannon
1. How to apply for the drug business license 1, the process of pharmaceutical business license processing process is as follows: (1) apply for application, submit an application to the provincial food and drug supervision and administration bureau where the location is located; ( 2) Submit the materials and submit materials related to the type of operation of the application; (3) The materials are corrected, the acceptance department is dealt with according to different circumstances, and the application unit is corrected; The review cycle is 30 working days; (5) Qualification issuance, and issuing drug business licenses for eligible units. It takes a long period of application to build. 2. Legal basis: Article 8 of the Drug Administration Law of the People’s Republic of China The head of the State Council ’s drug supervision and management department in charge of national drug supervision and management. The relevant departments of the State Council are responsible for supervision and management related to drug -related duties within their respective responsibilities. The drug supervision and management department of the State Council cooperates with the relevant departments of the State Council to implement the development planning and industrial policies of the national pharmaceutical industry. The drug supervision and management department of the people’s governments of the province, autonomous region, and municipality directly under the Central Government is responsible for the supervision and management of the administrative region. The departments of the municipal and county -level people’s governments of the district (hereinafter referred to as the drug supervision and management department) of the municipal and county -level people’s governments are responsible for the drug supervision and management of the administrative area. Relevant departments of local people’s governments at or above the county level are responsible for supervision and management related to drug -related drugs within their respective responsibilities. . Which materials need to be used for drug business license Id the following materials to apply for a drug business license: 1, pharmaceutical and medical device business license management system enterprise -side enterprise construction applications; 2. The qualifications of the legal representative of the enterprise and the person in charge of the enterprise, the original qualifications or the original title of the title, the copy of the title, and the resume of the personal resume; 3, the category and scope of the proposed drug; , Also submitted a copy of the “Drug Operation License”, “Business License” and asset -related certificates.
1. How to apply for the drug business license
1, the process of pharmaceutical business license processing process is as follows:
(1) apply for application, submit an application to the provincial food and drug supervision and administration bureau where the location is located;
( 2) Submit the materials and submit materials related to the type of operation of the application;
(3) The materials are corrected, the acceptance department is dealt with according to different circumstances, and the application unit is corrected; The review cycle is 30 working days;
(5) Qualification issuance, and issuing drug business licenses for eligible units. It takes a long period of application to build.
2. Legal basis: Article 8 of the Drug Administration Law of the People’s Republic of China
The head of the State Council ’s drug supervision and management department in charge of national drug supervision and management. The relevant departments of the State Council are responsible for supervision and management related to drug -related duties within their respective responsibilities. The drug supervision and management department of the State Council cooperates with the relevant departments of the State Council to implement the development planning and industrial policies of the national pharmaceutical industry.
The drug supervision and management department of the people’s governments of the province, autonomous region, and municipality directly under the Central Government is responsible for the supervision and management of the administrative region. The departments of the municipal and county -level people’s governments of the district (hereinafter referred to as the drug supervision and management department) of the municipal and county -level people’s governments are responsible for the drug supervision and management of the administrative area. Relevant departments of local people’s governments at or above the county level are responsible for supervision and management related to drug -related drugs within their respective responsibilities.
. Which materials need to be used for drug business license
Id the following materials to apply for a drug business license:
1, pharmaceutical and medical device business license management system enterprise -side enterprise construction applications;
2. The qualifications of the legal representative of the enterprise and the person in charge of the enterprise, the original qualifications or the original title of the title, the copy of the title, and the resume of the personal resume;
3, the category and scope of the proposed drug; , Also submitted a copy of the “Drug Operation License”, “Business License” and asset -related certificates.