Conditions for handling the business license of a pharmaceutical factory:
1. Shareholders meet the quorum; The registered shareholders of a limited liability company are generally limited to two or more and fifty or less; The registered shareholders of a one-person limited liability company are limited to natural person shareholders or corporate shareholders investors;
2. Shareholders' capital contribution reaches the minimum statutory capital; The initial capital contribution of all shareholders of the company shall not be less than 20% of the registered capital of the company, nor shall it be less than the statutory minimum registered capital of the company, and the rest shall be fully paid by shareholders within two years from the date of establishment of the company; Among them, the investment company can pay in full within five years; The minimum registered capital of a general limited liability company is RMB 30,000; The minimum registered capital of a one-person limited liability company is RMB100000 yuan, which must be paid in full at one time, but not in installments. Note: If the minimum registered capital of a limited liability company in a specific industry needs to be higher than the above-mentioned limit, it shall be stipulated separately by laws and administrative regulations. For example, the auction industry needs at least 6,543,800 yuan of registered capital; Pawnshops need at least 3 million registered capital;
3. Shareholders * * * jointly formulate the Articles of Association; Formulating the articles of association of a limited liability company is an important link in the establishment of the company. The Articles of Association is formulated by all investors on the basis of voluntary consultation. With the consent of all investors, shareholders shall sign and seal the articles of association.
4. Having a company name and establishing an organization meeting the requirements of a limited liability company; When a limited liability company is registered, its name shall conform to the provisions of the General Rules for the Names of Enterprise Legal Persons, and the words "limited liability company" or "limited company" must also be marked. The establishment of an organization meeting the requirements of a limited liability company generally refers to the shareholders' meeting, the board of directors, the board of supervisors, the manager or the shareholders' meeting, the executive director, one or two supervisors and the manager. There are many shareholders, the former is suitable for large-scale companies, and the latter is suitable for the opposite situation;
5. Have a company domicile; Having a fixed production and business operation place and necessary production and business operation conditions;
6. If the declared business project needs pre-approval, relevant licenses shall be provided.
To sum up, pharmaceutical factories need production license, business license, drug GMP certificate, drug approval number, environmental protection certificate, trademark, packaging filing, price approval, national tax registration and local tax registration. To set up a pharmaceutical production enterprise, it is necessary to apply to the pharmaceutical supervisory department where the enterprise is located, and have qualified pharmaceutical technicians, engineering technicians and corresponding skilled workers according to law; Then according to the local policy review, the state decides whether to agree or not.
Legal basis:
Article 8 of the Drug Administration Law of People's Republic of China (PRC)
The State Council drug supervision and administration department is in charge of the national drug supervision and administration. The relevant departments of the State Council are responsible for drug supervision and administration within their respective functions and duties. The drug supervision and administration department of the State Council cooperates with the relevant departments of the State Council to implement the national drug industry development plan and industrial policy. The pharmaceutical supervisory and administrative departments of the people's governments of provinces, autonomous regions and municipalities directly under the Central Government shall be responsible for the pharmaceutical supervisory and administrative work within their respective administrative areas. The departments responsible for drug supervision and administration of the people's governments at the city or county level divided into districts (hereinafter referred to as drug supervision and administration departments) shall be responsible for drug supervision and administration within their respective administrative areas. The relevant departments of the local people's governments at or above the county level shall be responsible for drug supervision and administration within the scope of their respective duties.