You are using an outdated browser and your browsing experience will not be optimal. Please update to the latest version of Microsoft Edge, Google Chrome or Mozilla Firefox. Install Microsoft Edge

July 1, 2022

Cambodia Issues Law on Food Safety

On June 8, 2022, the King of Cambodia promulgated the Law on Food Safety by virtue of Royal Kram S/RKM/0622/006, ushering in a new dawn for food safety, consumer protection and investment in the food industry in Cambodia. The law addresses the complete food chain from farm to table and is set to bring Cambodia in line with international food safety standards.

The Law on Food Safety addresses a range of key issues for the food and beverage industry including technical regulations and minimum requirements; import controls; labeling; and inspection, competent authorities, and penalties. The Ministry of Commerce is tasked with coordinating the implementation and enforcement of the law, in cooperation with four other key ministries.

Food Technical Regulations

The law provides a framework for issuing legislative instruments mandating standards (Food Technical Regulations) generally based on existing practices in Cambodia, or on a regional or international level.

The law provides the legal bases for adopting Food Technical Regulations and appoints institutions that may adopt or request to adopt them. We expect many new Food Technical Regulations will be issued in the near future.

Food Requirements and Minimum Food Requirements

The law provides the following minimum requirements for food (Minimum Food Requirements):

  • Food must be safe for consumption;
  • Food may not be imported, manufactured, processed, or sold in a fraudulent or deceptive manner;
  • Consumers must receive “adequate information” as defined in the law, including information on the food’s origin, ingredients, nutritional value, calorific content, user guidelines, and storage guidelines.
  • Food must meet the minimum hygiene, packaging, and labelling requirements detailed in the law;
  • Food classified as high-risk must be properly registered; and
  • Storage of food must meet the safety and quality conditions set by the competent ministries.

Relevant ministries may issue new laws and regulations setting further legal requirements for food (Food Requirements) in accordance with Food Technical Regulations (if extant).

Food producers, processors, or packers must ensure that their products meet all relevant Food Technical Regulations, Minimum Food Requirements, and Food Requirements.

Furthermore, these types of businesses may not produce:

  1. Food unsafe for consumption;
  2. Counterfeit food, or food without providing an expiration date;
  3. Food with packaging and labelling that does not meet Cambodian standards on food labelling;
  4. Food with packaging that does not identify the manufacturer’s name and date; or
  5. Food that violates the Law on Food Safety in any way, or other provisions in force, or store such foods.

Similar rules are set for wholesalers and distributors of foods, but with a focus on food storage and transport. Retailers are also subject to a minimum set of rules under the Law on Food Safety that is similar, but with a focus on food storage and sales.

Labelling, Advertising, and Hygiene Requirements

All pre-packaged foods must have labelling that meets all applicable Minimum Food Requirements, Food Requirements, other duly issued laws and regulations on labelling, and Cambodian standards on food labelling.

All food labels must also:

  1. Provide tracing information;
  2. Use Khmer language, or at minimum provide information relating to food safety and consumer protection in Khmer (which may be on an affixed Khmer-language sticker if the original label is not in Khmer);
  3. Identify the “adequate information” discussed above, including nutritional information;
  4. Not contain any information, images, or trademarks that contradict the required information on the label, or that is confusing or misleading to consumers; and,
  5. Be legible and visible to the consumer when purchasing (i.e., not be covered by its packaging).

The law prohibits all false, deceptive, and confusing food advertising, with respect to:

  • Product expectation;
  • Identity, type, nature, place of origin, physical quality, or nutritional quality;
  • Quality, ingredient, quantity, date of production;
  • Expiry date, usage guidelines, and terms;
  • Methods of sales, product availability, and price; and,
  • Other warranties or assurances regarding the product.

Other prohibited acts in advertising will be determined by the Ministry of Commerce and other relevant ministries as deemed necessary from time to time.

These provisions are in line with the Law on Consumer Protection, which prohibits similar false, deceptive, and confusing advertising regarding all types of consumer products.

Food hygiene requirements will be further set by implementing regulations, with the Law on Food Safety merely requiring food businesses to meet such requirements when issued.

Importation of Food

Imported foods must meet the Minimum Food Requirements and Food Requirements, and any requirements found in existing legislation.

Importers must provide an authorization certificate for imported foods, issued by the competent authorities of the exporting country, in accordance with risk management principles and pursuant to the applicable laws and relevant regulations of the exporting country.

The list of food products subject to this requirement, the required documentation, and any further importation requirements, will be determined by a sub-decree to be issued at a later date.

Laboratory analysis of imported foods may be required if the authorities deem it necessary.

Imported foods that are not compliant may be subject to:

  • Re-export;
  • Requirements for the importer to change the product to meet the legal requirements, including new labelling, followed by a re-examination; or,
  • Destruction.

All costs are incurred by the importer in these circumstances.

Food Inspection and Inspectors

This law authorizes food inspectors to inspect the market for compliance. Inspectors may inspect any type of food businesses and have powers to enter premises to do so. If necessary, they may take products for laboratory testing.

Lastly, the law outlines several penalties for violations, including fines and imprisonment. Stiff penalties apply to those who intentionally trade products containing harmful ingredients and chemicals, including up to 15 years imprisonment in cases that result in deaths.

Analysis

The Law on Food Safety, and the clarity it provides to the food industry and to consumers, is a welcome addition to Cambodia’s consumer protection regime. The adoption of this law is in line with the government’s recent focus on consumer protection, marked by the adoption of the Law on Consumer Protection, the Law on E-Commerce, and implementing regulations, such as the Prakas on Unfair Contract Clauses.

The most impactful immediate change for many food industry companies is that Khmer food labelling is now (at least partially) required, which was not standard practice in the market. Although the previous legal framework did require Khmer labelling, this regulation was either not clear, or was not duly enforced. We expect enforcement efforts to ramp up now that food inspectors have new powers of inspection and enforcement.

The requirement for nutritional values and calories on food labelling is also a substantial change to current practices, which will contribute greatly to the protection of consumers and will provide for a fairer playing field for businesses.

We eagerly await further implementing regulations surrounding imported foods, and especially further clarity on product registration requirements. It appears that registration of all types of pre-packaged food products is still required under existing laws and regulations. However, with the new law only addressing product registration requirements for high-risk products (and potentially imported products), we are keen to see how these registration requirements will be applied.

RELATED INSIGHTS​ 

June 19, 2026
For the first time, Thailand’s Food and Drug Administration (FDA) has published a consolidated list identifying all substances that have successfully passed its novel food safety evaluation process. The list is a step forward in regulatory transparency, but it also highlights a feature of the Thai regime that food companies often overlook: each approval is tied exclusively to the company that applied for it. A substance’s appearance on the list does not give other companies the green light to use it. This article examines the structure of Thailand’s novel food approval framework, the implications of applicant exclusivity, and the strategic choices it requires of food companies looking to bring novel ingredients to the Thai market. Thai FDA Food Safety Evaluation Framework Notification No. 376 of the Ministry of Public Health requires novel food substances to undergo a food safety assessment, with an exemption only for novel foods manufactured exclusively for export. The framework also encompasses “foods that do not qualify as novel foods” but which present characteristics warranting a safety evaluation, such as differing quality standards, increased serving sizes, or applications in specific food categories, where such changes affect consumption levels, nutritional value, or consumer safety. The recently published list of foods that passed the safety evaluation by the Thai FDA is structured by substance category and identifies the approved company (domestic manufacturer or importer), country of origin, substance name and trade name, approved purpose of use, and date of the Thai FDA’s approval notification certificate. A notable feature of Thailand’s novel food regime is that the approval result is tied exclusively to the company that submitted the application. Publication of the consolidated list does not constitute a general authorization to use the approved substances. The Thai FDA’s approval certificate specifies the approved conditions of use and the requirements
June 17, 2026
Thailand’s new labeling requirements for medical devices, which include for the first time a unique device identification (UDI) requirement for software as a medical device (SaMD), take effect on June 20, 2026. The Notification of the Ministry of Public Health regarding Criteria, Methods, and Conditions on Labeling and Instructions for Use for Medical Devices 2025, which replaces a similar notification from 2020, was published in the Government Gazette on December 22, 2025. To ensure clarity, modernity, and patient safety, the regulation requires domestic manufacturers and importers to provide labels and instructions for use (IFU) that are clearly legible, complete, and free of false or misleading claims. It also permits IFU to be provided in electronic format, such as via QR codes, websites, or other digital channels—directly relevant to SaMD, where physical labels are impractical and electronic presentation is the natural medium. The notification distinguishes two categories for labeling language. Home-use medical devices (for lay users outside healthcare facilities) must have labels and IFU in Thai. Professional-use medical devices may display labels and documentation in either Thai or English. This distinction is significant for SaMD developers: software intended for clinical professionals may use English-language interfaces and IFU, while consumer-facing health applications must provide Thai-language content. Labeling and UDI Requirements Labels and IFU must include, at a minimum: Product name and intended purpose Quantity or volume Name and address of domestic manufacturer or importer Thai FDA approval number Lot, version, or serial number Manufacturing date and expiry date For SaMD, the version number requirement is particularly relevant. The regulation also mandates display of a UDI code for SaMD in risk category 2 (moderate-risk), category 3 (moderate- to high-risk), and category 4 (high-risk), according to Thailand’s medical device risk classification system (which complies with the ASEAN Medical Device Directive and the EU
June 5, 2026
On May 25, 2026, Vietnam’s Ministry of Health issued Circular No. 16/2026/TT-BYT governing free-of-charge medicine support programs for medical establishments (Circular 16). Circular 16 will take effect on July 10, 2026, replacing Circular No. 31/2018/TT-BYT, which currently regulates the same subject matter. Circular 16 introduces several significant changes compared to the existing legal framework. Removal of Prior Approval Requirement Under the current regulations, free-of-charge medicine support programs are divided into two categories: (1) entirely free-of-charge provision of medicines for all types of drugs and (2) partially free-of-charge provision applicable only to brand-name drugs under patent protection or drugs whose generic products with identical active ingredients and dosage forms are available in Vietnam. Under the current regulations, partially free-of-charge programs are subject to mandatory registration with the competent authority, while entirely free-of-charge programs could be implemented without prior approval. A key reform under Circular 16 is that it stipulates only entirely free-of-charge medicine support programs applicable to all types of medicines, thereby eliminating the partially free-of-charge category. In addition, free-of-charge medicine support programs may be carried out solely based on a written agreement between the pharmaceutical company and the medical establishment, without any requirement for prior approval from competent authorities prior to implementation. Written Agreement Requirements Circular 16 requires the pharmaceutical company and medical establishment to enter into a written agreement in accordance with a prescribed template. This agreement must include the following compulsory information: Information on the supported medicines Form of support (entirely free-of-charge provision to patients) Quantity of medicines provided Target patient groups and applicable indications Duration of the program Rights and obligations of each party Transitional provisions on the protection of patients’ rights upon completion of the program The agreement may contain other contents as agreed by the parties, provided that these do not contradict applicable laws.
June 4, 2026
Indonesia’s Minister of Health has issued Decree No. HK.01.07/MENKES/301/2026 on the Affixation of Nutritional Labels and Health Information to Ready-to-Eat Processed Food Products. The decree came into force on April 14, 2026, and was issued to implement the Health Law and Minister of Health Regulation No. 3 of 2026 on Disease Control. The decree requires the inclusion of Nutri-Level labeling on the front-of-pack nutrition labeling (FOPNL) to indicate the product’s nutritional level based on the content of sugar, salt, and fat (“gula, garam dan lemak (GGL)”). Changes from 2024 Draft Regulation The Nutri-Level labeling was previously proposed in 2024 by the Indonesian FDA (BPOM) through a draft regulation concerning nutrition information. While the categories of Nutri-Level labeling remain the same in the issued decree, the content requirements of sugar, salt and fat in the decree are different from the earlier proposal introduced in the 2024 draft BPOM regulation. In addition, the decree has further specified that the content of fat in the Nutri-Level labeling is the content of saturated fat, not total fat as previously proposed in the 2024 draft. The decree requires Nutri-Level labeling to be implemented in beverage products, which is the same as previously proposed in the 2024 draft BPOM regulation. Other food products may gradually become subject to mandatory Nutri-Level labeling under future implementing regulations. Nutri-Level Labeling Food levels as shown by the Nutri-Level labeling are classified into four color-coded categories from A to D: Level A (lowest amount) in dark green Level B in light green Level C in yellow Level D (highest amount) in red The Nutri-Level labeling is represented by the following image. The requirements for each level for sugar, salt, and fat content, based on amounts per 100 milliliters of product in beverage form, are as follows. Nutri-Level information must be