How to legally sell homemade black plaster

The solution for legally selling homemade black plaster is as follows:

1. Apply for a patent or protect trade secrets to the relevant state organs. Self-made black plaster is actually an invention, and you can apply for a patent to the relevant state organs.

2. Improve the sales process. Selling homemade black plaster is also a market behavior, so we should actively handle the sales procedures.

When you sell the patent to a big pharmaceutical factory, you can ask to share the profits when signing the contract. The state has established an administrative license for the production and sale of drugs, and failed to obtain the corresponding qualifications and licenses in accordance with legal procedures, which is a minor administrative violation and a serious crime. Only manufacturers with legal sales qualifications can guarantee the smooth sales of goods. Only in this way can qualified plasters be sold safely and legally.

4. The law suggests strengthening the protection of secret recipe. In order to prevent the homemade secret recipe from being illegally stolen by others, we can consult the judicial organs and protect the ancestral secret recipe according to law.

5. Conduct legal advertising. The advertisement of homemade black plaster must be authentic. Never make false propaganda.

Legal basis:

"Good Quality Management Practice for Pharmaceutical Trading"

Article 7

The quality management department shall perform the following duties:

(a) to urge the relevant departments and post personnel to implement the laws and regulations on drug administration and this specification;

(two) to organize the formulation of quality management system documents, and to guide and supervise the implementation of the documents;

(three) responsible for the legality of suppliers and purchasers, the legality of purchasing drugs, and the legal qualifications of suppliers and purchasers' sales personnel, and dynamically manage according to the changes in the audit content;

(four) responsible for the collection and management of quality information, and the establishment of drug quality files;

(five) responsible for drug acceptance, guidance and supervision of drug procurement, storage, maintenance, sales, return, transportation and other aspects of quality management;

(six) to be responsible for the identification of unqualified drugs and supervise the treatment process of unqualified drugs;

(seven) responsible for the investigation, handling and reporting of drug quality complaints and quality accidents;

Responsible for reporting counterfeit and inferior drugs;

(nine) responsible for drug quality inquiry;

(ten) responsible for guiding the setting of computer system quality control functions;

(eleven) responsible for the audit of computer system operation authority and the establishment and update of basic data of quality management;

(twelve) to organize the verification and calibration of relevant facilities and equipment;

(thirteen) responsible for drug recall management;

(fourteen) responsible for the report of adverse drug reactions;

(fifteen) to organize the internal audit and risk assessment of the quality management system;

(sixteen) to organize the inspection and evaluation of the quality management system and service quality of drug suppliers and buyers;

(seventeen) to organize the examination of the transportation conditions and quality assurance ability of the entrusted carrier;

(eighteen) to assist in quality management education and training;

(nineteen) other duties that should be performed by the quality management department.

Regulations for the implementation of the drug administration law

essay

An application for establishing a pharmaceutical production enterprise shall be submitted to 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. The pharmaceutical supervisory and administrative departments of the people's governments of provinces, autonomous regions and municipalities directly under the Central Government shall, within 30 working days from the date of receiving the application, organize the acceptance according to the starting conditions stipulated in Article 8 of the Drug Administration Law; Those who pass the inspection shall be issued a pharmaceutical production license.