今天和20世纪90年代对杀菌剂的监管要求。

P. Halleux
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引用次数: 2

摘要

本文将回顾欧洲引入新物质的监管要求,并说明美国和日本存在的差异。注册要求存在于欧共体的每个成员国,对于使用现有或新的杀菌剂活性成分的新配方的每种类型的申请,将用例子来描述。还将描述影响杀菌剂活性成分使用的拟议EEC指令。将讨论制剂指令对含有杀菌剂的制剂的影响。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Regulatory demands for biocides today and in the 1990s

This paper will review the regulatory requirements for the introduction of new substances in Europe and illustrate where differences exist in USA and Japan.

Registration requirements, which exist in every member state of the EEC for each type of application for new formulations using existing or new biocide active ingredients, will be described with examples. Proposed EEC directives which affect the use of biocide active ingredients will also be described.

The impact of the Preparations Directive for formulations containing biocides will be discussed.

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