Select Committee on European Scrutiny Fourteenth Report


1 Nutrition and health claims made on foods


(24763)

11646/03

COM(03) 424

Draft Regulation on nutrition and health claims made on foods

Legal baseArticle 95 EC; co-decision; QMV
DepartmentFood Standards Agency
Basis of considerationSEM of 11 March 2004
Previous Committee ReportHC 63-xxxiii (2002-03), para 18 (15 October 2003)
To be discussed in CouncilJune 2004
Committee's assessmentPolitically important
Committee's decisionFor debate in European Standing Committee C; further information requested

Background

1.1 According to the Commission, as food production has become more complex, consumers are increasingly interested in the information appearing on food labels, and in their diet. It therefore takes the view that this information should be clear, accurate and meaningful. Current Community legislation[1] lays down a number of detailed rules on food labelling, including a prohibition on the attribution of properties which prevent, treat and cure ailments, but these provisions are open to different interpretations, leading to numerous discrepancies.

1.2 Against this background, and a recent case in which the European Court of Justice interpreted the existing legislation as banning all health claims relating to human diseases,[2] the Commission put forward in July 2003 this draft Regulation, which would maintain the existing general approach, but allow nutrition and health claims under strict conditions. Only those claims which conform with the Regulation would be allowed for foods placed on the Community market, and the proposal would apply, not just to "traditional" nutrients, but to other substances with a nutritional effect, and to all foods. Particular attention would be paid to claims which, although factually true, can be misleading.[3]

1.3 More specifically, the proposal would establish:

  • a positive list of permitted nutrition terms, such as "low", "rich" and "light", and the conditions under which they may be used; and
  • procedures for the pre-market authorisation of health claims, under which the European Food Safety Agency (EFSA) would be consulted on the supporting scientific evidence before an authorisation was given.

It would also require the Commission to establish nutrient profiles for foods which may carry nutrition or health claims, and lay down the basis on which the claims of different products may be compared. In addition, certain categories of health claims, such as those which refer to general non-specific benefits, or to psychological and behavioural functions, would be prohibited; and it would also be prohibited for foods not specifically designed for weight control to make claims relating to potential weight loss.

1.4 In our Report of 15 October 2003, we noted that the Government was broadly supportive of the proposal, pointing out that there had been an increase in claims of this sort on the UK market, but that their validity or otherwise was not apparent to consumers, and had presented difficulties for enforcement authorities. Although a voluntary approach had been encouraged in the UK with some success, it was clear that the coverage had been patchy, and that statutory action at Community level was needed. However, it would be important to establish appropriate transitional arrangements, bearing in mind the time required to compile and submit applications.

1.5 We also noted that a Regulatory Impact Assessment was being prepared, and that the proposal would have significant resource implications for the EFSA, particularly in the short term. We therefore said that we thought it sensible to await this Assessment before taking a firm view, and that, in the meantime, we would continue to hold the document under scrutiny.

Supplementary Explanatory Memorandum

1.6 In her supplementary Explanatory Memorandum of 11 March 2004, the Parliamentary Under-Secretary of State for Public Health at the Department of Health (Miss Melanie Johnson) says that the Government's position remains essentially as we reported in last October, and that the negotiations "appear to be on track". She does, however, say that the Government will be:

  • pressing the Commission to adopt a proportionate approach when it establishes, within the framework to be set by the Council, the detailed criteria for nutrient profiling;
  • seeking to allay any industry concern that the prohibition on certain types of health claim could stifle innovation;
  • pressing for longer transitional periods so as to minimise any costs incurred by businesses in complying with the proposal, and in particular so that any re-labelling can be achieved within the 24 month or so timescale used by industry for routine changes to product lines; and
  • aiming to ensure that "healthy option" products offered by most major retailers, which make a clear nutrition claim and meet the relevant criteria, will not be adversely affected by any of the other provisions of the proposal.

1.7 The Minister has also provided the promised Regulatory Impact Assessment, though she says that the financial implications of the proposal will be explored further as the negotiations progress, and the Assessment updated accordingly. In the meantime, the Assessment suggests that the products most likely to be affected by the proposal are those bearing health claims, particularly in the food supplements sector, which, although not banned by the proposal, could nevertheless become commercially unviable if the claims in question are not allowed.[4] However, it is not possible at this stage to quantify the likely consequences either in this area, or as regards the effects of nutrient profiling, though the Assessment suggests that the range of products carrying claims is likely to decrease, that, although substitute marketing may be possible, this could lead to a reduction in the number of producers or importers, and that the costs of developing new products may increase.

1.8 On the other hand, it also suggests that the quality of the remaining products (as measured by their ability to deliver the claimed health and nutritional benefits) is likely to improve substantially, and that this will bring considerable benefits to the consumer. In addition to these, and to the public health benefits arising from better information, free movement of goods within the internal market would be facilitated and there would be increased legal security for economic operators.

Conclusion

1.9 Although the Minister has said that the negotiations on this proposal appear to be on track, we note that there are a number of outstanding concerns, and that some of the uncertainties — for example, on nutrient profiling — will not be resolved until after it has been adopted. We also note that, notwithstanding any health benefits, there are concerns that the proposal will decrease the range of nutritional products available and discourage innovation.

1.10 We believe that these issues require further consideration, and we are therefore recommending that the proposal be debated in European Standing Committee C. We hope that it will be possible before then for the Government to provide an updated Regulatory Impact Assessment, and in any event we ask for the Government's assessment of the likely effect of the proposal on employment.


1   Directive 2000/13/EC.OJ No. L 109, 6.5.00, p.29. Back

2   C-221/00, Austria v. Commission. Back

3   Such as "90% fat-free", which masks a fat content of 10%. Back

4   The UK has also questioned whether specific prohibitions are necessary, bearing in mind that health claims would need to be approved by the EFSA. Back


 
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