Day: 28/04/2025

Argentina – ANMAT announces new amendments to the Argentine Food Code related to mycotoxins, food additives, and cider

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The National Administration of Drugs, Food, and Medical Technology (ANMAT in Spanish) has announced new amendments to the Argentine Food Code, related to: Mycotoxin Limits (Article 156 of the CAA): – – —

  • Mycotoxin limits are incorporated into Article 156 for certain food categories. Mycotoxins are toxic compounds produced by certain types of fungi that grow in various foods under specific conditions. They are heat-stable and resistant, persist during the milling, washing, and processing of food products, and can enter the food chain directly. Joint Resolution No. 15/2025 of the Secretariat of Health Management and the Secretariat of Agriculture, Livestock, and Fisheries.

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  • Additive Labeling (Chapter V of the CAA): The criteria between the Food Code and Mercosur regulations regarding the labeling of additives are harmonized. Joint Resolution No. 16/2025 of the Secretariat of Health Management and the Secretariat of Agriculture, Livestock, and Fisheries.
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  • Cider and Incorporation of Pear Cider (Article 1085 of the CAA): The articles on the definition, characteristics, and labeling of apple cider, as well as products made with cider, are updated. Cider obtained exclusively from pear must is incorporated into the Argentine Food Code, and sparkling ciders, musts, and added products are classified. In addition, the definition and physical and chemical characterization of pear cider are incorporated. Joint Resolution No. 17/2025 of the Secretariat of Health Management and the Secretariat of Agriculture, Livestock, and Fisheries.

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Argentina – Article 1396 on labeling of food additives of the Argentine Food Code has been repealed

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By means of Joint Resolution 16/2025, the Secretariat of Health Management and Secretariat of Agriculture, Livestock Farming and Fishing repealed Article 1396 of the Argentine Food Code.

The Ministry of Health of Rio Negro requested the repeal of Article 1396 of the Argentine Food Code (CAA), since it is in conflict with the STANDARDS FOR FOOD LABELING AND ADVERTISING, Joint Resolution SPRyRS No. 149/2005 and SAGPyA No. 683/2005, which incorporates Resolution Grupo Mercado Común (GMC) No. 26/03 “Mercosur Technical Regulations for Labeling of Packaged Foods” and renders the aforementioned article null and void.

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Mexico – Congresswoman asks Cofepris to ban the additive erythrosine (red dye3)

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During a session of the State Congress, a resolution proposed by Deputy Beatriz Fraustro was approved, urging the Federal Commission for the Protection Against Sanitary Risks (COFEPRIS) to take the necessary actions and conduct studies to promptly address the ban on the additive known as erythrosine or E-127 in the production and sale of both domestic and imported food and beverages.

The legislator noted that the United States Food and Drug Administration (FDA) recently prohibited the use of Red 3 dye in food, beverages, and ingestible medications.

She elaborated that this additive is a synthetic dye derived from petroleum, commonly used to impart a bright cherry red color to food and beverages.

For further information, you can access the original source in Spanish

Brazil – Anvisa has temporarily halted the integration with the Siscomex Unified Portal for food imports

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The National Health Surveillance Agency (ANVISA in Portuguese) informs the temporary suspension of the implementation schedule of the integration of its systems with the Single Foreign Trade Portal (Siscomex in Portuguese) for food imports, previously announced.

The decision was taken due to the identification of systemic inconsistencies in the integration flow and in the status of requests in the Single Portal. New dates for the implementation of the integration will be announced in due course.

During this period, the protocols already completed will continue to be analyzed by ANVISA, being the importer’s responsibility to monitor the final status of each LPCO (license, permit, certificate and other documents – Siscomex Single Portal module that allows requesting documents required for foreign trade operations).

In addition, it is recommended that food import processes be re-registered through the Solicita system, using the LPCO I00046 model, without integration with the Single Portal, in accordance with the guidelines of the LPCO Manual.

Colombia – INVIMA introduces new guidelines for the depletion of food and beverage labels

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The National Institute for Food and Drug Surveillance (INVIMA in Spanish) informs all stakeholders that guidelines have been established for the process of depleting labels and using adhesives on food and beverages, in accordance with Resolution 5109 of 2005 and 810 of 2021.

The requirements were set forth in resolution 2025013945. This administrative act introduces significant changes compared to the previous procedure, aiming to enhance clarity, efficiency, and proportionality in the regulation for users of the health system:

  • Depletion without prior authorization: For the first time, it is permitted that, in specific cases where there is no health risk or error in the product’s nature, labels can be depleted without the need for prior authorization from Invima. This measure aims to reduce unnecessary administrative burdens on the entity, facilitating the legal marketing of products with minor labeling errors.
  • Authorizations with a defined timeframe: In instances where prior authorization is required, it will be granted for a single period of 18 months through a duly justified administrative act.
  • Individual analysis for unaddressed cases: Situations not explicitly covered by the new resolution will be evaluated on a case-by-case basis to ensure a technical, consistent, and fair application of the regulation.

It is important to note that there will be no changes to the cost of the process or the time taken to review applications. This ensures that regulatory adjustments do not impose additional burdens on industry stakeholders. Through this resolution, Invima reaffirms its commitment to advancing a technical, proportional health regulation that serves public health and development.

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