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Food Supplement Registration in EuropeonUnion

EuropeonUnion

✓ The registration of food supplements in the European Union is a crucial process that ensures the safety and quality of products available to consumers. In order to be placed on the market, manufacturers must provide detailed information on the composition, labeling, and intended use of their supplements. This information is carefully reviewed by regulatory authorities to verify compliance with EU regulations and to protect public health.

✓ The registration process involves submitting a comprehensive dossier that includes scientific data supporting the safety and efficacy of the supplement. This includes toxicological studies, stability testing, and clinical trials, where applicable. Manufacturers must also demonstrate that their products are manufactured in compliance with Good Manufacturing Practices (GMP) to ensure consistency in quality and safety standards.

✓ Once a food supplement is registered, it is subject to ongoing monitoring to ensure continued compliance with EU regulations. Regular inspections of manufacturing facilities and product testing are conducted to verify that products meet the required standards. Non-compliance can result in penalties, including fines and product recalls. By enforcing strict registration and monitoring procedures, the European Union aims to provide consumers with confidence in the safety and quality of food supplements available on the market.

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