-
DE
The EU Novel Food authorisation process regulates which new foods may be safely marketed in the EU. It is governed by Regulation (EU) 2015/2283.
The EU Novel Food authorisation process regulates which new foods may be safely marketed in the EU. It is governed by Regulation (EU) 2015/2283.
Novel foods are foods and food ingredients that were not used for human consumption to a significant degree within the European Union before 15 May 1997. The EU Novel Food authorisation is the official approval procedure that ensures such products are assessed for safety, nutritional value, and consumer suitability before they can be placed on the market.
The legal basis is Regulation (EU) 2015/2283 of the European Parliament and of the Council, which has been in force since 1 January 2018, replacing the earlier Regulation (EC) No 258/97. The regulation applies across all EU member states and is implemented by the European Commission in cooperation with the European Food Safety Authority (EFSA).
The novel food category is broad and covers a wide range of product groups:
The process for obtaining EU novel food authorisation is clearly structured and involves several key steps:
Food business operators or applicants submit a complete application to the European Commission via the central online portal. The application must include comprehensive scientific data on the safety, composition, production process, and proposed conditions of use of the product.
The EFSA (European Food Safety Authority) conducts an independent scientific risk assessment. This covers aspects such as toxicity, allergenicity, nutritional value, absorption behaviour, and potential interactions. EFSA typically has nine months to deliver its opinion.
Based on the EFSA opinion, the European Commission, together with the member states, decides on the authorisation. If approved, the product is added to the Union list of authorised novel foods, which is publicly accessible.
Authorised novel foods are subject to specific labelling requirements. For example, foods containing insect-derived ingredients must carry allergen warnings. All labelling must be transparent and understandable for consumers.
For foods that have a documented history of safe use in a non-EU country, known as traditional foods from third countries, Regulation (EU) 2015/2283 provides for a simplified notification procedure. In these cases, it is sufficient to demonstrate at least 25 years of safe use in a country outside the EU.
An important aspect of the current authorisation framework is data protection for applicants: newly submitted scientific data can be protected for a period of up to five years. During this time, no competitor may use this data in their own application without the consent of the original applicant.
The novel food authorisation has direct relevance for public health. It ensures that new food products pose no risk to consumers before they reach the market. At the same time, it enables innovation in the food industry that can contribute to food security, sustainability, and meeting evolving nutritional needs.
For Healthy Oral Flora & Dental Care
Formulated lozenges with Dentalac®, lactic acid bacteria, and Lactoferrin CLN®
For Healthy Oral Flora & Dental Care
Formulated lozenges with Dentalac®, lactic acid bacteria, and Lactoferrin CLN®
For your universal protection
As one of the most valuable proteins in the body, lactoferrin is a natural component of the immune system.
For your iron balance
Specially formulated for your iron balance with plant-based curry leaf iron, Lactoferrin CLN®, and natural Vitamin C from rose hips.