19

2014-11

Explanation of "The Drug Administration Law of the People's Republic of China"

On September 20, 1984, the Seventh Meeting of the Standing Committee of the Sixth National People's Congress passed the "Drug Administration Law of the People's Republic of China" (hereinafter referred to as the "Drug Administration Law"), which came into effect on July 1, 1985.

19

2014-11

Explanation of "Measures for the Implementation of the Drug Administration Law of the People's Republic of China"

On January 7, 1989, the State Council approved the "Implementation Measures of the Pharmaceutical Administration Law of the People's Republic of China" (hereinafter referred to as the "Implementation Measures"), which was promulgated and implemented by the Ministry of Health on February 27 of the same year.

19

2014-11

Explanation of "New Drug Approval Measures"

Drugs have a special and important relationship with human life and health, especially when new drugs are used in clinical treatment of various diseases, sufficient experimental data must be provided to prove their safety,

19

2014-11

Explanation of "Administrative Measures for Narcotic Drugs"

In the process of long-term production and the struggle with pain, human society has continuously discovered some drugs that can act as anesthesia

31

2020-08

Explanation of "Administrative Measures for Medical Toxic Drugs"

On December 15, 1988, the 25th executive meeting of the State Council passed the "Measures for the Administration of Toxic Drugs for Medical Use" (hereinafter referred to as the "Measures"), which was promulgated and implemented on December 27 of the same year.

19

2014-11

Explanation of "Medicine Packaging Management Measures"

Pharmaceutical packaging is directly related to the quality of medicines and the convenience of patients' safe medication. If the quality of the packaging personnel,

19

2014-11

Explanation of "Pharmaceutical Production Quality Management Regulations"

The original Good Manufacturing Practice of "Pharmaceutical Manufacturing Practice" (hereinafter referred to as "Specification") is referred to as GMP.