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Chinese guidelines for copy biologicals Posted 21/11/2014

Last update: 6 April 2018

Since 2003, the China Food and Drug Administration (CFDA) (simplified Chinese: 国家食品药品监督管理局) is the Chinese authority that oversees all drug manufacturing, trade, and registration.

CFDA is in charge of comprehensive supervision on the safety management of food, health food, and cosmetics and is the competent authority of drug regulation in Mainland China.

The Chinese Government’s establishment of a single drug regulatory authority was an important step toward foreign access, because it eliminated the conflicting standards that prevailed among provincial government agencies, centralized the Chinese healthcare regulatory system, and made it more transparent. CFDA now oversees all medications, both Western and Traditional Chinese Medicines (TCM), as well as advertising.

CFDA administers the Drug Administration Law, which came into effect on 1 December 2001.

Applications from domestic applicants are handled according to the procedures and requirements for new drugs or generic drugs, whereas applications from overseas applicants are handled according to those for imported drugs.

On 29 October 2014, the Chinese Center for Drug Evaluation (CDE), which is part of CFDA, published draft copy biologicals guidance [1]. A finalized technical guidance for the development and evaluation of copy biologicals was released on 28 February 2015 [2].

1. Overarching guidelines
This guideline covers all copy biologicals products:

Technical Guideline for Development and Evaluation of copy biologicals (interim)
Date: 28 February 2015
www.fdanews.com/ext/resources/files/03-15/03-15-China-Biosimilars.pdf?1425486653

2. Draft overarching guidelines
This guideline covers all copy biologicals:

Draft guidance for research and evaluation techniques for copy biologicals
Released for consultation: 29 October 2014
End of consultation: 29 November 2014
www.cde.org.cn/zdyz.do?method=largePage&id=212

The Chinese guidelines mainly follow the European Medicines Agency (EMA) approach. Similarly to the US and EU regulatory authorities, the CDE expects a detailed structural and functional characterization of the copy biological when comparing it to the reference product. The CDE also takes a similar step-wise approach to examine comparability through comparative pharmacology data, non-clinical studies and clinical studies. 

The final Technical Guideline sets forth basic principles for the technical review of copy biologicals, the criteria for establishing biosimilarity and the conditions under which extrapolation of indications is permissible. The guideline also clarifies some outstanding questions, such as the approval pathway for copy biologicals compared to originator biologicals, and adopts less stringent requirements, for example, in the definition of a copy biological and its reference product.

Domestic copy biologicals have been on the market in China for over 25 years, according to data from the Southern Medicine Economic Research Institute (SMEI) of CFDA. The first recombinant human interferon beta 1 was launched in 1989. Domestic erythropoietins, granulocyte colony-stimulating factors and monoclonal antibodies are also commercialized in China. The country has approved 382 genetically engineered drugs and genetically engineered vaccines, but only 21 products are innovative and the rest are copy biologicals, according to SMEI data [1].

Related article
China releases draft biosimilars guidance

EU guidelines for biosimilars

Reference
1. GaBI Online - Generics and Biosimilars Initiative. China to release biosimilars guidelines [www.gabionline.net]. Mol, Belgium: Pro Pharma Communications International; [cited 2014 Nov 21]. Available from: www.gabionline.net/Guidelines/China-to-release-biosimilars-guidelines
2. Derbyshire M. Regulation of copy biologicals in China . Generics and Biosimilars Initiative Journal (GaBI Journal). 2018;7(2): [Epub ahead of print]

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Source: CDE, CFDA

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