The reason for the revision is to unify the method of labeling the country of origin (font size) for imported processed foods and domestic processed foods in order to alleviate the burden on companies and solve the problem of equity, clarify the…
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The Panel on Food Additives and Flavourings (FAF) was requested to assess the safety of xanthan gum (E 415) for its uses as a food additive in food for infants below 16 weeks of age belonging to food category (FC) 13.1.5.1.
According to the EU Authority's expert opinion, it is appropriate to change the usage guidelines for Yarrowia lipolytica yeast biomass because the proposed change is secure under the suggested conditions of use.
Based on the evidence presented, the EU Authority has determined that the proposed use of cellobiose is safe.
Permission to clear imported food and drug products, medical devices and supplies Pesticides and everything related to the authority's field of work, after conducting the necessary examinations and analyses, falls within the executive tasks…
The Saudi Food and Drug Authority has issued the following recommendations:
1) Documentation confirming the organic status of the products in question (such as a copy of the relevant certification).
In accordance with TZS 742 standard, Containers for raw Brazil nut kernels must be produced from food-grade packing material and sealed in a way that protects the product's sanitary, safe, nutritional, and organoleptic qualities.
In accordance with TZS 742 standard, Containers for both raw and roasted hazelnut kernels must be made of food-grade packing material and sealed in a way that protects the product's sanitary, safe, nutritional, and organoleptic qualities.
In accordance with TZS 330 standard, Almond flour must be packaged in containers made from food grade packing material and sealed in a way that prevents contamination and maintains the product's freshness, safety, nutritional value, and sensory…
The Secretary of Health and Human Services has the authority to issue regulations outlining what constitutes good manufacturing practice for dietary supplements, per section 402(g) of the Federal Food, Drug, and Cosmetic Act (FD&C Act) (21 U.…