20 19 medical and health laws and regulations: classification of counterfeit drugs and inferior drugs

? 20 19 Tianjin Hospital Recruitment | Physical Examination Announcement and Publicity Summary (continuously updated)

Firstly, the definitions of counterfeit drugs and counterfeit drugs are introduced: the ingredients contained in drugs are inconsistent with those stipulated in national drug standards; Passing off non-drugs as drugs or passing off other drugs as drugs. Summarized as? Fake drugs are not drugs? .

The teacher summarized the classification of counterfeit drugs as follows:

1. ingredients counterfeit drugs: including those whose ingredients are inconsistent with the national drug standards, pass off as non-drugs as drugs.

2. Procedural counterfeit drugs: refers to drugs that do not meet the statutory requirements, are prohibited by the state, are produced without the approval of the state or have not been tested, or the raw materials are produced without approval.

3. Drugs that no longer have medicinal value: deteriorated and contaminated drugs are counterfeit drugs.

4. Does not have the claimed medicinal value: those beyond the prescribed scope are counterfeit drugs.

Let's talk about inferior drugs. If the content of drug ingredients does not meet the national drug standards, it is inferior. Summarized as? Bad medicine is not good medicine? . Inferior medicine is real medicine, but it has defects.

1. Failure to indicate or change the validity period;

2 do not indicate or change the production batch number;

3. Exceeding the validity period;

4. The packaging materials and containers that are in direct contact with drugs are not approved;

(5) Adding colorants, preservatives, spices, correctants and auxiliary materials without authorization;

(six) other do not meet the requirements of drug standards.

It is concluded that during the validity period, the packaging containers and accessories do not meet the drug regulations and are inferior drugs.

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