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China new classification system for chemical drug NMPA registration ( 2016 version)

Tags: | NMPA | Pharmaceuticals | Drug | 药监局 | 医药品 | 药品 |



On March 4, 2016, China Food and Drug Administration (CFDA) issued a new regulation - “the Work Plan for Reforming Chemical Drugs Registration Classification System “;

The New Classification System (2016 version) changed the previous chemical drug classification system (2007 version) and sets forth new registration requirements for applicants.

Under the New Classification System, chemical drugs are classified into 5 categories, Below is an overview of the new classification system:

Classification Definition / Scope Monitoring period

Class 1: Innovative new drugs which have never been marketed within or outside China,

Active ingredients and their formulations which have clinical value and contain compounds with new structures and pharmacological effects.

5 years

Class 2: Improved new drugs which have never been marketed within or outside China

2.1 - Drug substances or preparations which contain optical isomers of the known active ingredients by using the splitting or the synthesis method; turn known active ingredients into ester or salt (including salt containing hydrogen bonds or coordination bonds); change the acid radical, alkali base or metal element of the known active ingredients of salts; or turn into other non-covalent bond derivatives (such as complex chelate or inclusion compound), which also have an obvious clinical advantage.
2.2 - New drug preparations using the new dosage form (including the new drug delivery system); the new prescription process or the administration route for known active ingredients, and with an obvious clinical advantage.
2.3 - New compound preparations of known active ingredients, which also have an obvious clinical advantage.
2.4 - New preparations of known active ingredients with new indications.

2.1- 3 years
2.2- 4 years
2.3- 4 years
2.4- 3 years

Class 3: Domestic Drugs which imitate innovative drugs that have not been marketed within China but have been marketed outside of China

Drug substances or preparations that have the same active ingredients, dosage forms, strengths, indication, administration route, usage and dosage as innovative drugs.

0 year

Class 4: Domestic Drugs which imitate innovative drugs that have been marketed within China

Drug substances or preparations that have the same active ingredients, dosage forms, strengths, indication, administration route, usage and dosage as innovative drugs.

0 year

Class 5: Imported Drugs which have been marketed outside China, apply china domestic market approval.

5.1 - Innovative drugs (including drug substances or preparations) that that have been approved outside China.
5.2 - Non-innovative drugs (including drug substances or preparations) that that have been approved outside China.

0 year


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不同类型的GACC注册,海外申请人可以根据自身情况,选择不同的渠道进行注册申请。
1. 如果你精通GACC注册流程,可以直接向中国海关提交免费申请,其网站为:www.customs.gov.cn or www.singlewindow.cn;
2. 如果你是第一次申请,不清楚GACC注册的程序h流程,申请文件要求等,可以通过CRA中国代理机构渠道申请注册,CRA会提供专业的注册咨询服务,帮助你顺利通过GACC注册审查,尽快获得GACC注册号。

Different types of GACC registration, overseas applicants can choose different channels to apply for :
1. If you specialise in the GACC registration process, you can submit a free application directly to China Customs, website: www.customs.gov.cn or www.singlewindow.cn;
2. If you are not clear about the registration process of GACC registration, application document requirements, etc., you can apply for registration through the channel of CRA (Chinese Representative Agency) , CRA will provide professional registration services to help you successfully pass the GACC registration review and get the GACC registration number quickly.
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