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[对健康有益?欧洲健康声明法规中科学证实要求的分析]

[Good for your health? An analysis of the requirements for scientific substantiation in European health claims regulation].

作者信息

Todt Oliver, Luján José Luis

出版信息

Salud Publica Mex. 2016 Jun;58(3):393-8.

Abstract

OBJECTIVE

To identify the various types of evidence, as well as their relative importance in European health claims regulation, in order to analyze the consequences for consumer protection of the requirements for scientific substantiation in this regulation.

MATERIALS AND METHODS

Qualitative analysis of various documents relevant to the regulatory process, particularly as to the implications of the standards of proof for the functional food market, as well as consumer behavior.

RESULTS

European regulation defines a hierarchy of evidence that turns randomized controlled trials into a necessary and sufficient condition for health claim authorizations.

CONCLUSIONS

Consumer protection can be interpreted in different manners. High standards of proof protect consumers from false information about the health outcomes of functional foods, while lower standards lead to more, albeit less accurate information about such outcomes being available to consumers.

摘要

目的

识别各类证据及其在欧洲健康声明法规中的相对重要性,以便分析该法规中科学依据要求对消费者保护的影响。

材料与方法

对与监管过程相关的各类文件进行定性分析,尤其关注证据标准对功能性食品市场及消费者行为的影响。

结果

欧洲法规定义了证据的层级结构,将随机对照试验作为健康声明授权的必要且充分条件。

结论

对消费者保护的解读方式可能各异。高标准的证据保护消费者免受有关功能性食品健康效果的虚假信息影响,而较低标准则使消费者能获取更多关于此类效果的信息,尽管这些信息准确性较低。

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