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Laws & Regulations - Drugs - Drug Administration Law of the Peoples Republic of China
Drug Administration Law of the Peoples Republic of China
 
2011/7/4 9:05:07¡¡Source: ¡¡Hits:

Order of the President of the Peoples Republic of China
(No. 45)
The Drug Administration Law of the People¡¯s Republic of China, revised at the 20th Meeting of the Standing Committee of the Ninth National People¡¯s Congress on February 28, 2001, is hereby promulgated and shall go into effect as of December 1, 2001.
                                                   Jiang Zemin
                                                       President of the People¡¯s Republic of China
                                                      February 28, 2001

DRUG ADMINISTRATION LAW OF THE PEOPLE¡¯S REPUBLIC OF CHINA
   (Adopted at the 7th Meeting of the Standing Committee of the Sixth National  Peoples Congress on September 20, 1984, revised at the 20th Meeting of the Standing Committee of  the Ninth National Peoples Congress on February 28, 2001)
CONTENTS
Chapter I   General Provisions
Chapter II   Control over Drug Manufacturers
Chapter III   Control over Drug Distributors
Chapter IV   Control over Pharmaceuticals in Medical Institutions
Chapter V    Control over Drugs
Chapter VI   Control over Drug Packaging
Chapter VII   Control over Drug Pricing and Advertising
Chapter VIII   Inspection of Drugs
Chapter IX    Legal Liabilities
Chapter X     Supplementary Provisions
Chapter I
General Provisions
Article 1 This Law is enacted to strengthen drug administration, to ensure drug quality and safety for human beings, to protect the health of people and their legitimate rights and interests in the use of drugs.
Article 2 All institutions and individuals engaged in research, production, distribution, use, or drug administration in the People¡¯s Republic of China shall abide by this Law.
Article 3 The State develops both modern and traditional medicines to give full p

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