The new EC Regulation on nutrition and health claims on foods

A. Reuterswärd
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引用次数: 10

Abstract

The area of health claims has been unregulated in Europe until recently. A new regulation on nutrition and health claims made on foods came into force on 19 January 2007. The Regulation has been eagerly awaited by all parties involved. The Regulation includes 37 whereas clauses, 29 Articles and an annex for nutrition claims and conditions applying to them. In practice, three main types of health claim are included in the Regulation, as referred to in Articles 13 and 14. The type of the scientific evidence is described slightly differently for Article 13.1 and Article 13.5: ‘‘generally accepted scientific evidence’’ and ‘‘newly developed scientific evidence’’, respectively, although the scientific status of evidence shall be the same for all kinds of claims. So far, there are four types of guidance for applying the Regulation. The wording of health claims is an essential issue in the Regulation, as well as the concept of nutrient profiles. In the Regulation there are three issues of special interest, when compared to the Swedish Food Sector’s Code of Practice, i.e. concerns about ‘‘other substances’’, ‘‘food supplements’’ and ‘‘the average consumer’’. The Regulation will be evaluated in 2013, reporting the impact of this Regulation on dietary choices and the potential impact on obesity and non-communicable diseases.
欧盟关于食品营养和健康声明的新法规
直到最近,健康声明领域在欧洲一直不受监管。一项关于食品营养和健康声明的新法规于2007年1月19日生效。有关各方都热切期待该条例的出台。该规例包括37条附属条款、29条及一份有关营养声称及其适用条件的附件。实际上,如第13条和第14条所述,该条例包括三种主要类型的健康声明。第13.1条和第13.5条对科学证据的类型的描述略有不同:分别是“普遍接受的科学证据”和“新开发的科学证据”,尽管各种主张的证据的科学地位应相同。到目前为止,适用该规例的指引有四种。健康声明的措辞以及营养成分的概念是该条例的一个重要问题。与瑞典食品部门的业务守则相比,该条例中有三个特别关注的问题,即对“其他物质”、“食品补充剂”和“普通消费者”的关注。2013年将对该条例进行评估,报告该条例对饮食选择的影响以及对肥胖和非传染性疾病的潜在影响。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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