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CFDA Announces Draft Regulation to Implement China's New Food Safety Law

On December 9, China Food and Drug Administration (CFDA) released the draft Regulation on the Implementation of the Food Safety Law of the P.R. China1 (hereinafter "Regulation") for public comments by January 8, 2016. This extensive Regulation includes 200 articles, detailing issues surrounding the implementation and enforcement of the Food Safety Law (hereinafter "Law"), which entered into force in October of this year. This draft Regulation, once adopted, will have a significant impact on overseas food producers and operators, especially for those in the industry of health food and infant formula. It also further defines some key terms to the food industry, e.g., edible agricultural product, food in special dosage forms with unified consumption amount, food repacking, and food in bulk.

In the next few weeks, we will walk you through important sections of the Regulation and focus on different topics. This issue will provide you with a snapshot of the articles in the Regulation that will likely have a major impact on the food import business, particularly foods imported into China that have been under a high level of scrutiny, such as health food and infant formula.

I. Government Management of Imported Food

The Regulation is designed to establish a management system of food import per food category and safety risk level, taking into account various factors (e.g., food safety risk, safety control capability of the enterprise, and food safety condition of the exporting country/region).2 For food, food additives and food related products3 at high risk level, samples will be retained and tested under entry inspection; for products with ordinary risk, sampling testing will be carried out; and for products with low risk, only on-site inspections will be conducted.4

Food incidents taking place overseas (e.g., food recall in foreign countries) may result in further control measures (e.g., import restriction, import suspension, goods returned or destruction, etc.) by the Chinese authorities.5

II. Foreign Food Producers, Exporters and Chinese Food Importers

The Regulation also sheds more light on product compliance by foreign food producers/exporters and local importers. For example, Article 112 requires foreign food producers/exporters to prevent any deliberate destruction by others to food and edible agricultural products via chemical, biological or physical means at different stages of food production and operation (e.g., raw material control, production, packaging, storage and transportation, etc.).

Furthermore, local food importers are under an obligation to establish a regime to audit the food producer and exporter overseas.6 Details regarding the design and function of the audit system can be found in the Administrative Measures for the Audit and Inspection of Overseas Companies by Food Product Importers (draft for comment)7 published by the General Administration of Quality Supervision, Inspection and Quarantine (AQSIQ) in September this year. In short, the draft Measures impose heavy responsibilities on the local importer to ensure the safety of food products that they plan to distribute in China. At least once in every three years, domestic food importers are obliged to conduct on-site audit of facilities outside of China that produce, for example, health food, infant formula, formulation food for special medical purposes and meat products. Such on-site inspection can be authorized to an accredited third party.

III. Specially Controlled Food Products

According to the amended Law, pre-market approval (i.e., notification or registration) from the Chinese Government is a prerequisite to the distribution and operation of health food, infant and young children formula food and foods for special medical purposes (hereinafter "specially controlled food products") in China.

The Regulation uses the term 'food in special dosage form with unified consumption amount' to capture all food in the form of capsule, tablet, liquid oral dosage, medicinal granules, etc., which is subject to a pre-set daily intake amount or consumption amount.8 We expect to see more detailed rules published by the Chinese government in the future in terms of its regulation of food in special dosage form.

a. Health Food

The Regulation further clarifies some issues in the existing rules targeting health food. In particular, not only does the Regulation explicitly block the use of the novel food registration procedure to clear an ingredient reserved for health food use, it also provides details of the to-be-published inventory of food ingredients for health food use . Specifically, the inventory will include specifications for the ingredient name, the use level, manufacturing process, functional components and test methods. Further, an ingredient that differs substantially from the ingredient listed (resulting from extraction and purification) will be deemed new, thus, is excluded from the scope of the inventory under Article 81.

With regard to imported products, "health food imported for the first time" suggests no health food made per the same formula has been imported from the same country and the same producing company in the past.9 When the health food is imported for the first time, it must be registered with CFDA in advance, unless it falls under the scope of vitamins and minerals, which are only subject to notification procedures. Once the notification number is issued to a health food to be imported, the actual import must be carried out within three months and the proof of customs clearance as well as the testing report must be filed with the food and drug administration at the provincial level.10

To register a health food product, sample products must be manufactured in a plant which has implemented Good Manufacturing Practice (GMP).11 As to the product claim, it must strictly follow the language set forth in the function claim catalogue and no alteration is allowed.12 Health food that shares the same registration certificate or filing number shall use the same trademark.13

b. Infant and Young Children Formula

Since infant and young children formula food have repeatedly fallen under the spotlight in various food scandals in China, the Regulation includes many articles intended to address issues related to the production and operation of infant formula as well as product registration/notification procedures.

More specifically, the Regulation requires infant and young children formula to be developed in accordance with Chinese regulations and standards. In principle, one company shall not have more than 3 series of products and 9 product formula. Substances that are subject to optional additions (e.g., choline, inositol, taurine in infant formula) cannot be reflected in the product name of infant and young children formula.14 Imported formula of milk powder for infants and young children, per Article 96, must be registered.

Further, prior to the marketing of infant and young children formula food, the producer must notify relevant authorities of the information regarding product raw materials, food additives, formula and product label.15 Article 47 imposes an obligation for review of formulation registration certificate on the operator of infant and young children formula where applicable.

IV. Food Labeling

Given a large amount of noncompliant food issues arise from the product label, the Regulation elaborates on food labeling issues in various chapters. Of particular note is the proposed prohibition of sticker use on imported food products. Under the draft Regulation, all prepackaged food must be directly printed with a Chinese label before it is imported to China.16 Additionally, food shall not be labeled with any pre-set amount of consumption or designated daily consumption, unless it is a health food, infant and young children formula food or foods for special medical purposes.17

Claims such as "non addition of" or "non-use of" substances that are prohibited in pertinent food safety national standards are to be banned. For example, colostrum is currently banned in infant formula.18 Accordingly, under the draft Regulation, "no addition of colostrum" is not a permitted claim on the label of an infant formula milk powder product. Similarly, GMO food or raw materials that have not yet been approved by the Chinese government shall not bear a "non-GMO" label.

The draft Regulation, for the first time, clearly defines "defects with food label," which refers to non-compliance which has no impact on food safety and will not mislead consumers in their safe consumption of food (e.g., spacing between letters, font size, use of simplified or traditional characters and rounding intervals, etc.).19 Under the updated Law, a food label with a defect no longer constitutes a cause for consumer compensation of ten times the purchasing price or three times the loss.20 However, food labels or instruction manuals non-compliant with food safety national standards can become the subject of a Class III food recall even if no health damage is expected.21 Notably, under a Class III recall, a food possessing a non-compliant label can continue to be sold as long as the label is fixed, mitigation measures have been taken to guarantee product safety, and public notice has been given about the mitigation measures.22

V. Cross-border E-Commerce

Nowadays, "cross-border e-commerce" (CBEC) has become a term commonly used in the food industry, particularly as it relates to the import and export of food to China. The Regulation, under Article 117, explicitly mandates food imported via CBEC shall follow the Law and the Regulation. In the meantime, the Regulation authorizes the quality supervision inspection and quarantine department under the State Council with other relevant departments to jointly establish the rules for supervision and management of imported food, food additives and food related products via CBEC.23

In fact, this October, AQSIQ published Supervision and Management Rules for the Safety of Imported Food via Cross-border E-commerce in Online Shopping Bonded Mode (draft for comment)24 to regulate the operation and safety supervision of imported food that is delivered to bonded warehouses via CBEC and then redistributed to Chinese consumers upon individual orders.

VI. Food Repackaging and Toll Manufacturing

Food repackaging is a very common practice among food importers and distributors, and the Regulation newly defines this action and establishes some restrictions. Notably, at the stage of food operation, if food in large packs is redistributed into small units for sale without repackaging, it does not fall under the definition of "food repackaging."25 When a food operator repackages food, no modification to the production date or extension of the shelf-life is permitted.26

In the toll manufacturing of food or food additives, while the toll manufacturer must obtain a production license and be responsible for the production activity, the company procuring the tolling service is ultimately responsible for the food safety.27

VII. Transportation

Following up on the amended Food Safety Law, which expands its scope of regulation to cover food transportation and storage, the Regulation in several articles focuses on the qualification of logistic companies and warehouses in the food business. Food companies doing business in China should carefully select their local partners. By way of example, food producers/operators are obligated to examine the storage/transportation company's capability in guarantying food safety.28 A written contract must be reached in commissioned food storage and transportation, describing each party's obligations to comply with the food safety requirements in China.29


 

1http://www.sda.gov.cn/WS01/CL0050/137340.html
2Article 105
3 'Food related product', under the Law, refers to food packaging materials, containers, detergent, disinfectant, utensils and equipment for food production and operation.
4 Article 109
5 Article 116
6 Article 110
7http://www.aqsiq.gov.cn/gzcypt/cazxyj/20150908_5/wyyj/
8 Article 195
9 Article 195
10 Article 84
11 Article 115
12 Article 88
13 Article 93
14 Article 92
15 Article 87
16 Article 114
17 Article 78
18 Letter by the General Office of Ministry of Health in Response to Question Regarding Applicable Standard for Colostrum Products, available at: http://www.nhfpc.gov.cn/sps/s3594/201204/4556d47bdde141d19e82d8253ae02af...
19 Article 195
20 Article 125 and Article 148 , Food Safety Law
21 Article 65
22 Article 66
23 Article 117
24http://www.aqsiq.gov.cn/gzcypt/cazxyj/20151013/wyyj/
25 Article 195
26 Article 75
27 Article 34
28 Article 49
29 Article 52 

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David J. Ettinger, Keller Heckman, Partner, Food and Drug Corporation, International Trade Lawyer, Attorney, Shanghai, China
Partner

David Ettinger joined Keller and Heckman in 1999. Mr. Ettinger represents domestic and foreign corporations in the area of food and drug law.

Mr. Ettinger relocated to Keller and Heckman's Shanghai office in November 2012 to focus on the Asian market and counsel companies in the Far East on food, drug, and chemical regulatory matters. He has extensive experience counseling clients on product development and product protection of food and drug packaging in the United States, Europe, Asia, Canada, and South America. From 2006-2007, Mr. Ettinger...

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Jenny Li, Keller Heckman, China Food, Drug Regulation, Shanghai, International Trade
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Jenny Li joined Keller and Heckman in October 2007.

Ms. Li counsels clients on regulatory issues focusing on food and drug, with an emphasis on regulatory regimes in the Asia-Pacific region. She also counsels clients on food labeling, food claims, food additives, as well as, important issues regarding food imports in Asian countries.

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Mark Thompson, Keller Heckman, EU Regulatory Compliance, Asian markets Lawyer, Attorney, Shanghai, China
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Mark Thompson joined Keller and Heckman in 2008 as an Associate with the firm’s Washington, DC office.  During that time, Mr. Thompson assisted clients in demonstrating compliance with U.S. and EU regulations pertaining to food, food packaging, drugs, as well as applicable environmental requirements.  In October 2009, Mr. Thompson transferred to Keller and Heckman's office in Shanghai, China, after which he expanded upon his practice to capture regulatory compliance matters in various Asian markets.   He currently advises a wide array of businesses and trade associations...

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Wilfred Feng, Keller Heckman, registration programs, herbicide development scientist, Consultant, Shanghai, China
Scientist

Wilfred Feng joined Keller and Heckman in 2005.

Mr. Feng provides technical assistance to clients on regulatory issues focusing on food and drug regulation and chemical control laws in Asia, including food additives, food labeling, food packaging, dietary supplements, drugs, medical devices, cosmetics, pesticides, bioengineered products, and industry and specialty chemicals.

Mr. Feng has an extensive background in regulatory affairs, government affairs, marketing, and project management and has worked in several...

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Chen Hu , Keller Heckman, Scientist, Food Chemistry, Regulatory Compliance, Shanghai
Scientist

Chen Hu joined Keller and Heckman in April 2009. He provides technical assistance in the area of food, food packaging, and chemical control, in matters related to regulatory compliance in Asian-Pacific regions.

Mr. Hu works closely with government authorities and trade associations in various phases of regulatory development. Mr. Hu has prepared and submitted hundreds of Chinese applications for registration of food packaging materials, food additives, new food ingredients, and new chemical substances. He is experienced in auditing plant...

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