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​ 

August 10, 2026
On June 17, 2026, Indonesia’s National Agency of Drug and Food Control (BPOM) issued BPOM Regulation No. 10 of 2026 on Nutritional Information on Processed Food Labels. The new regulation, which revokes three previous nutrition labeling regulations, introduces several notable changes affecting food and beverage manufacturers, importers, and distributors. These changes range from updated nutrient reference values and serving-size requirements to the introduction of the Nutri-Level front-of-pack labeling system for certain beverage products. Businesses operating in Indonesia should carefully review these developments and assess their products’ compliance with the new requirements during the transition period. Implementation of the Nutri-Level Labeling System To implement the recently issued decree on Nutri-Level labeling, BPOM Regulation No. 10 of 2026 stipulates the requirements to implement the Nutri-Level labeling system on the front-of-pack. Under the new framework, ready-to-drink beverages, powdered beverages, and liquid or solid concentrates are required to display Nutri-Level labeling on the front label of their packaging. The Nutri-Level labeling system classifies products into color-coded levels A through D based on their sugar, sodium, and total fat content. The applicable Nutri-Level is determined based on the lowest level measured in the assessment of sugar, sodium, and total fat content. For products classified as level C or D, the Nutri-Level label must be accompanied by information on the relevant sugar, sodium, and total fat content per 100 ml of the ready-to-consume product. Products classified as level A or B may either display only the Nutri-Level designation or display the Nutri-Level together with the relevant nutritional information per 100 ml. Minimum Vitamin and Mineral Content Required for Declaration BPOM Regulation No. 10 of 2026 introduces a stricter threshold for the declaration of vitamins and minerals in the nutritional value information section (ING). Vitamins or minerals may only be declared if they are present at a
August 10, 2026
The drug registration process in Vietnam will be simplified, particularly for foreign applicants, following the recent issuance by Vietnam’s Ministry of Health (MOH) of a new circular that is expected to reduce administrative hurdles. Circular No. 32/2026/TT-BYT on the registration of drugs and medicinal ingredients (Circular 32) was issued on July 29, 2026, and will take effect on October 1, 2026, replacing Circular No. 12/2025/TT-BYT. Key provisions of the new circular are discussed below. Five-Year Data Exclusivity and Five-Month Public Disclosure Framework Circular 32 updates data protection guidelines by explicitly referencing Article 128 of the amended Intellectual Property Law, which sets out that new drugs supported by clinical trial data submitted for the first time will be granted a five-year data exclusivity period from the date of the initial marketing authorization (MA) approval. Subsequent applications that rely on the originator’s protected data will not be eligible for approval from the date of submission of the originator’s registration dossier until five years after the first MA is granted. Furthermore, in accordance with the new regulations, the regulatory authority must publicly disclose information on subsequent applications five months before the granting of MA, providing originator companies with an opportunity to exercise and enforce their intellectual property rights. Simplified Requirements for Foreign Legal Documents Circular 32 expands the circumstances under which legal documents issued by foreign authorities are exempt from consular legalization and authenticity verification requirements. Specifically, such documents may be exempt if the Drug Administration of Vietnam (DAV) is able to verify their authenticity directly through official electronic means, including written confirmation or email correspondence sent directly to the MOH by the competent foreign authority, or publicly accessible English-language databases maintained by recognized foreign regulatory authorities. In addition, the new circular permits the submission of electronic notarized copies of legal documents
July 24, 2026
As food innovation continues to accelerate, manufacturers are increasingly introducing ingredients derived from new sources, produced using novel technologies, or lacking a significant history of human consumption. While these innovations create new opportunities for the food industry, they also raise important questions regarding consumer safety. For this reason, many jurisdictions, including Thailand, the European Union, Australia and New Zealand, Canada, and Singapore, require a premarket safety assessment for novel food ingredients before they can be placed on the market. The objective of this assessment is to ensure that each ingredient is safe for its intended use and level of consumption, does not present toxicological, allergenic, microbiological, or nutritional concerns, and will not mislead consumers. Scientific authorities typically evaluate the ingredient’s identity, manufacturing process, composition, specifications, anticipated dietary exposure, toxicological information, nutritional impact, and history of use before determining whether it can be marketed. Against this background, the Thai Food and Drug Administration (FDA) recently took an important step toward improving regulatory transparency by publishing, for the first time, a consolidated public list of substances that have successfully completed the Thai FDA’s safety assessment process, including substances determined to be novel foods and those determined not to fall within the novel food category. The list identifies the approved substances, the corresponding manufacturers or importers, approval dates, and the approved conditions of use. Although the publication does not change the existing legal framework governing novel food approvals, it provides businesses with greater visibility into the Thai FDA’s regulatory precedents and the types of substances that have previously been accepted through the safety assessment process. The full announcement is available on the Thai FDA’s website. As the list is now publicly available, it also provides useful insight into the types of substances that have successfully completed the Thai FDA’s safety assessment process.
July 24, 2026
For businesses in Thailand’s regulated industries, the problem of “too many licenses” is one of the most familiar hurdles to getting a product to market. Take a simple example: importing the materials necessary to sell teriyaki chicken skewers. To legally do this, a business may need approvals from several different agencies—separate permits for the chicken (Department of Livestock Development), the dipping sauce (Thai FDA), the wooden skewers (Department of Forestry), and other ingredients, each under a different authority. This kind of overlap is often cited to argue for a “regulatory guillotine”—a systematic review to cut outdated or duplicative rules that slow investment and business activity. The Facilitation of Licensing and Public Service Consideration Act B.E. 2569 (2026) (Licensing Facilitation Act 2026) is Thailand’s most significant response yet to that concern. This article looks at the Facilitation Act 2026 through a life sciences and regulatory affairs lens—what it may mean for the manufacturers, importers, and distributors of food, drugs, medical devices, cosmetics, and similar products who routinely deal with several regulators to bring a single product to market. The Super License: One Approval Standing in for Many The reform with the clearest potential for regulated-product businesses is the law’s “super license” mechanism, referred to as a “main license” in the statute. Once a business obtains the main license for a regulated activity, it is automatically deemed to hold all related sublicenses issued by other agencies for that same activity, provided the activity has been designated as eligible in the Government Gazette. The Licensing Facilitation Act 2026 also creates a central application center, allowing applicants to submit a single application and pay all relevant fees at one point of contact, with the center routing the application to each agency through a shared information system. The potential benefits of this for businesses