How to tell whether a medicine is real or fake?

Drugs imported without formal import procedures and approval are considered counterfeit, and illegal trading is illegal.

According to Article 39 of the "Drug Administration Law", the import of drugs must be reviewed by the drug regulatory department of the State Council. Only after the review is confirmed to be in compliance with quality standards, safe and effective, can the import be approved and issued to the importer. Drug registration certificate.

For medical units with urgent clinical needs or small quantities of imported drugs for personal use, import procedures must be handled in accordance with relevant national regulations.

According to Article 142 of the Criminal Law of the People's Republic of China and the People's Republic of China, whoever produces and sells inferior drugs causing serious harm to human health shall be sentenced to fixed-term imprisonment of not less than three years but not more than ten years, and A fine of not less than 50% but not more than twice the amount of the sales amount shall be imposed.

If the consequences are particularly serious, the person shall be sentenced to fixed-term imprisonment of not less than ten years or life imprisonment, and shall also be fined not less than 50% but not more than twice the sales amount, or have property confiscated. The term "substandard drugs" as mentioned in this article refers to drugs that are inferior drugs in accordance with the provisions of the "Drug Administration Law of the People's Republic of China".

Extended information

According to Article 15 of the "Drug Administration Law", the following conditions must be met to open a pharmaceutical business enterprise:

1) Have qualifications recognized in accordance with the law Pharmaceutical technicians;

2) Have business premises, equipment, storage facilities, and sanitary environment suitable for the drugs they operate;

3) Have business premises, equipment, storage facilities, and sanitary environments suitable for the drugs they operate;

Quality management agencies or personnel;

4) Have rules and regulations to ensure the quality of the drugs they operate.

Article 16 Pharmaceutical trading enterprises must operate pharmaceuticals in accordance with the "Pharmaceutical Distribution Quality Management Practices" formulated by the drug regulatory department of the State Council in accordance with this Law.

The drug regulatory department shall certify whether pharmaceutical operating enterprises meet the requirements of the "Good Manufacturing Practice for Pharmaceutical Distribution" in accordance with regulations; and issue certification certificates to those who pass the certification.

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