GMARegulatory updates for supplements and ingredients.
A selection of documents, opinions and changes from institutional sources, with the context required to understand their potential impact.
A radar for institutional sources.
Every update identifies the date, responsible authority and original document. Operational implications remain distinct from the regulatory text.
Revised requirements on characterisation, manufacturing, exposure, genotoxicity and environmental safety for applications submitted from 20 July.
The European project addresses risks associated with supplements other than vitamins and minerals and identifies priorities for further investigation.
Regulation (EU) 2026/391 modifies the conditions of use and specific labelling requirements for the Novel Food.
The route from pre-submission through scientific assessment and publication of the opinion.
This material is editorial and does not constitute legal or regulatory advice. Every application must be verified against the specific ingredient, product, market and available documentation.
From news
to application.
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