- Novel Foods in Europe: How to Determine Status and Achieve Market Authorization
- EU News on Food Supplement Regulations
- The novel food evaluation process delays access to food innovation in the European Union
- The Key Point of the New EFSA Novel Food Guidance
- Novel foods in Europe: Opportunities, challenges and new demands from The EFSA
- Quality of food supplements – Europe
Service details
Our process includes the following steps
Regulatory audit and adjustment
An analysis of the regulatory status of active ingredients, additives and verify the dosages
Rules of labelling
A review of all mandatory information and also add specific warning(s) aligned to each ingredient used
Marketing claim analysis
A review of all the nutritional and health claims permitted for use on labelling and marketing tools
Validation of label compliance
Product notification in sold countries
We will prepare and submit of files for notification in the targeted countries in accordance with local regulations, with prior registration in other countries if necessary, to enable the mutual recognition process. We will proactively follow up until authorization is granted and provide you with proof of filing, notification, or a notification certificate
Transmission of an authorization proof
