An increasing number of foods sold in the EU bear nutrition and health claims. A nutrition claim states or suggests that a food has beneficial nutritional properties, such as “low fat”, “no added sugar” and “high in fibre”. A health claim is any statement on labels, advertising or other marketing products that health benefits can result from consuming a given food, for instance that a food can help reinforce the body’s natural defences or enhance learning ability.
In December 2006 EU decision makers adopted a Regulation on the use of nutrition and health claims for foods which lays down harmonised EU-wide rules for the use of health or nutritional claims on foodstuffs based on nutrient profiles. Nutrient profiles are nutritional requirements that foods must meet in order to bear nutrition and health claims. One of the key objectives of this Regulation is to ensure that any claim made on a food label in the EU is clear and substantiated by scientific evidence.
- Regulation 1924/2006 on nutrition and health claims made on foods
- Commission Regulation No 353/2008 establishing implementing rules for applications for authorisation of health claims
- Commission Regulation No 1169/2009 amending Regulation (EC) No 353/2008 establishing implementing rules for applications for authorisation of health claims
EFSA’s work includes providing scientific advice on:
- General function health claims under Article 13.1 of the EU Regulation
- Claims regarding disease risk reduction and child development or health under Article 14 of the EU Regulation
- Criteria for setting nutrient profiles
EFSA is responsible for verifying the scientific substantiation of the submitted claims, some of which are currently in use, some of which are proposed by applicants – companies who want to submit claims for authorisation in the EU. This information serves as a basis for the European Commission and Member States, which will then decide whether to authorise the claims.
Guidance for applicants and engagement with stakeholders
EFSA has prepared guidance on how to submit claims applications, following an extensive consultation process with industry and other interested parties.
EFSA has been engaging regularly with stakeholders to outline and clarify where needed the process followed by the NDA Panel in the evaluation of claims, and has been providing guidance in this field since 2007 through guidance, briefing documents and the holding of scientific meetings.
What is a health claim?
What is a nutrition claim?
What are nutrient profiles?
What are EFSA’s tasks under the Regulation?
The European Commission is required to draw up a “positive list” of the many well-established “general function” health claims in the EU, such as “calcium is good for your bones”, on the basis of claims submitted by the EU Member States. This type of health claims, dealt with under Article 13.1 of the Regulation, include those referring for instance to growth, development and the functions of the body and to psychological and behavioural functions, but not to the reduction of disease risk nor to child development or health which are separately addressed under Article 14 and Article 13.5 of the Regulation.
EFSA is providing scientific advice to support this process. So far, EFSA has published 125 opinions providing scientific advice for more than 900 health claims, out of the draft a list of 4,637 health claims submitted to EFSA by the Commission between July 2008 and March 2010.
The list of authorised health claims will be adopted progressively by the European Commission and Member States taking into account EFSA’s opinions.
More information on Article 13.1 claims
2. To give an opinion on individual applications for health claims
New “function” health claims
In addition to those claims included in the positive list of permitted “general function” health claims, applicants can submit dossiers to the Member States in order to seek a risk assessment from EFSA on new function claims for a specific product. For these claims which are based on newly developed scientific evidence, protection of proprietary data can be requested. These claims as referred to in Article 13.5 of the Regulation, will be transmitted to EFSA by competent authorities in Member States and will be assessed on a case-by-case basis by EFSA’s NDA Panel. The applicants shall present more complete evidence in a structured manner for their specific products. EFSA is required to deliver these opinions within five months.
Summary of Art 13.5 claims applications received by EFSA
Claims regarding disease risk reduction and child development or health
These include claims relating to reduction of disease risk or to child development or health, which are dealt with under Article 14 of the Regulation. Any such claims submitted for inclusion in the EU positive list have to be examined by EFSA and approved by the Commission and Member States. EFSA is to verify that the health claim is substantiated by scientific evidence, delivering its opinion within 5 months of validating the applications received. The applicant is requested to present more complete evidence in a structured manner for their specific products.
Summary of Art 14 claims applications received by EFSA
3. To provide guidance on the preparation of applications for the authorisation of health claims
EFSA is an organisation committed to openness, transparency and dialogue. One of the ways it demonstrates this commitment is through its activities with stakeholders.
In July 2007, EFSA’s NDA Panel has published guidance for applicants on the submission of health claims for authorisation. The guidance, developed following public consultation, aims to help companies who want to submit health claims for authorisation. It addresses the types of information to include in the application, in particular concerning the scientific data and evidence required to support claims. In September 2009, EFSA has also provided further guidance to applicants in this area by publishing a revised Frequently Asked Questions (FAQs) document. This document takes into account the experience gained with the evaluation of health claims applications, comments received through the consultation held in May 2009, as well as the comments received from applicants at a technical meeting in June 2009 on Article 14 and 13.5 health claims.
How to submit an application
4. To give scientific advice on nutrient profiles
EFSA’s task is to provide scientific advice that could be used by EU policy makers in establishing nutrient profiles. EFSA’s NDA Panel delivered the main elements of its scientific advice in a Scientific Opinion on nutrient profiles adopted on 31 January 2008. This first step will help inform the Commission and Member States in deciding which nutrient profile system to implement. EFSA will continue supporting the Commission in its ongoing work to establish a final nutrient profiling system. To this end, EFSA developed a new tool to assist EU risk managers in testing different nutrient profile scenarios - a tailor-made food composition database compiled in co-operation with Member States and industry. The database was delivered to the European Commission in July 2008.
Where can I find more information on EFSA’s work in the area of health claims?
Where can I find more information on the Regulation?
European Commission: Questions and Answers on health and nutrition claims