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An interesting rulemaking, if you like that sort of thing

机译:一个有趣的规则制定法,如果您喜欢这种事情

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In today's column, I try to persuade you that the way FDA has lately been making regulations is unusual, surprising, and interesting. Yes, I know how that sounds. But the regulations are crucially important to food companies, so it's useful to watch them develop and perhaps even get involved. The typical sequence for agencies making regulations (OK to call them "rules") is, first, they issue a proposed regulation, inviting the public to comment on it. Second, they mull over all the comments, make changes to the proposal as they see fit, and third, issue the final regulation, revised perhaps in light of the comments, together with detailed explanations of why they did what they did. Fourth, the final regulation becomes effective at some date after its publication. Watchers of the FDA's seven separate proposed regulations growing out of the Food Safety Modernization Act were surprised in September, because FDA didn't follow the typical sequence. They had been proposed, and had been commented upon by the public. But instead of issuing final versions of the regulations, which was the expected next step, FDA issued slightly revised proposed versions of four of them.
机译:在今天的专栏中,我试图说服您FDA最近制定法规的方式是不寻常,令人惊讶和有趣的。是的,我知道这听起来如何。但是,法规对于食品公司至关重要,因此,观察它们的发展甚至参与进来是很有用的。机构制定法规的典型顺序(可以称其为“规则”)是,首先,它们发布拟议法规,邀请公众对此进行评论。其次,他们考虑了所有评论,对提案进行了适当的修改,第三,发布了最终法规,可能根据评论进行了修订,并详细解释了他们为什么这样做。第四,最终法规在其发布后的某个日期生效。九月份,由于《食品安全现代化法案》出台的FDA七项拟议法规的观察者感到惊讶,因为FDA没有遵循典型的程序。已经提出了这些建议,并已得到公众的评论。但是,FDA并未发布法规的最终版本,而这是下一步的预期,而是发布了对其中四个法规的修订版本。

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