I need approvals for 2 supplements. Liquid Detox product and NADH supplement, in accordance to EU legislation. can you send me the link of particular requirement needed by EU for labeling and other legal parameter of these products. Thanks
I understand that the labels need to e adjusted to each local market, but how about licensing the supplemenet itself? Are synthetic food supplements allowed? If the supplement is authorized in one EU country - does that mean that this authorization is valid in the whole EU (i understand that label needs to be approved country by country bases)?
Hello! The label must comply with the specific regulations of each country. Therefore, the label must be reviewed for each country. The food supplement must also be notified in each country. Currently there is no global notification for all of Europe, but rather you have to go country by country. I hope this information is useful to you.
It won't be great translating the label for every single country if we are a "single market". In the case the product is sold to all the EU countries only through a website, should the label still be translated to every single language and can the translated information in the website or leaflet for example satisfy these requirements?
Hello! It is necessary that the label be in the official language of the country in which it is going to be sold. You can make a label per country or a multi-label where all languages appear.
Hello! No, it is not necessary to market the product. but if the product is inspected, the sanitary inspection can make an analysis and if it is shown that there is fraud, it can constitute a crime and an administrative infraction.
