According to Article 10 of the E-commerce Law of the People's Republic of China, e-commerce operators shall register market entities according to law. However, unless individuals sell their own agricultural and sideline products and household handicraft products, individuals do not need to obtain permission according to law, nor do they need to register according to laws and administrative regulations.
Twelfth e-commerce operators engaged in business activities, need to obtain the relevant administrative license according to law, should obtain the administrative license according to law.
Article 13 The commodities sold or services provided by e-commerce operators shall meet the requirements of protecting personal and property safety and environmental protection, and shall not sell or provide commodities or services prohibited by laws and administrative regulations.
Precautions:
1. First, you need to register and submit a series of reports to sfda, such as factory address, scale and preparation type, in order to get approval.
2. Various facilities must be perfect, including clean material warehouse, temporary warehouse, finished product warehouse, processing workshop, processing equipment, laboratory, etc. , must have specific figures, need to be approved.
3. The bacteria detection in the clean area should meet the preparation requirements. The clean area for preparing decoction pieces is 300,000, and the laboratory standard is at least 1 0,000. If the sterile area is about 500 square meters, the cost is about 6,543,800 yuan.
4. After the above content is qualified, it will be reviewed, which is also called GMP review. The verification time is generally about 2 days.
5. Those who pass the GMP certificate can be legally produced and sold.
Extended data:
Measures for the Administration of Drug Business License Article 6 The implementation standards for the establishment and acceptance of drug wholesale enterprises shall be formulated by China Food and Drug Administration.
The implementation standards for the establishment and acceptance of pharmaceutical retail enterprises shall be formulated by the food and drug supervision and administration departments of all provinces, autonomous regions and municipalities directly under the Central Government in accordance with the relevant contents of these Measures and the Quality Management Standards for Pharmaceutical Trading, and reported to China Food and Drug Administration for the record.
Article 7 Approval of the business scope of pharmaceutical trading enterprises. Business scope: narcotic drugs, psychotropic drugs and toxic drugs for medical use; Biological products; Chinese herbal medicines, Chinese herbal pieces, Chinese patent medicines, chemical raw materials and their preparations, antibiotic raw materials and their preparations, biochemical drugs.
To engage in drug retail, we must first check and verify the business category, determine the applicant's qualifications for dealing in prescription drugs and over-the-counter drugs, clarify the business scope, and then check and verify the specific business scope.
The examination and approval of toxic drugs, narcotic drugs, psychotropic drugs, radioactive drugs and preventive biological products for medical use shall be carried out in accordance with the relevant state regulations on the management of special drugs and preventive biological products.
References:
Phoenix Finance-Is it legal to sell medicinal materials online? Traditional Chinese medicine
Baidu Encyclopedia-E-commerce Law of the People's Republic of China