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Regulatory Status

How is TG declared on the label of a final food in EU and why?

Specific labeling is unnecessary from regulatory viewpoint. Different from food additives, there is no technological effect or function of the enzyme in the final product in general. TG in ACTIVA® preparation is not an exception, has no technological effect in the final product due to the fact that the enzyme is inactivated during production process of finished product (mostly by heating) or the substrate of the enzyme has been depleted even if the residues are technologically unavoidable.

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Labelling of foodstuffs made with the enzyme Transglutaminase
The regulatory status of the enzyme transglutaminase in the processing of raw and heated meat products in Germany
Is there any legislation governing TG in EU?
How is TG positioned in France and Denmark?
How is TG positioned in other countries?
What is a processing aid?
Recommended labeling when ACTIVA® EB/ACTIVA® PB is used in Germany
How is TG declared on the label of a final food in EU and why?
 
AJINOMOTO’s position – the Bundesrat requested the Federal Government for a clear labelling
Is transglutaminase necessary to be declared as an allergen within the scope of Directive 2000/13EC?
Is transglutaminase produced by GMO?
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