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Administrative guidance on submission of dossiers and assessment reports for the peer-review of pesticide active substances and on the maximum residue level (MRL) application procedure

机译:关于提交少人和评估报告的行政指导,对杀虫剂活性物质和最大残留水平(MRL)申请程序的同行评审报告

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This document provides guidance to applicants submitting dossiers related to the approval of pesticide active substances and for setting of maximum residue levels, and to Member States preparing assessment reports on active substances within the scope of Regulation (EC) No 1107/2009 and Commission Implementing Regulation (EU) 2020/1740, or evaluation reports on maximum residue levels applications, within the scope of Regulation (EC) No 396/2005. It describes the administrative requirements for the preparation and submission of the dossier to support an application for the approval, the amendment of approval or the renewal of an existing approval of a pesticide active substance, and for maximum residue levels,for applications submitted as of 27 March 2021.It also describes the support initiatives available from the preparation of the application (pre-submission phase) to the adoption and publication of EFSA's output. The Transparency Regulation amended the General Food Law by introducing new provisions in the pre-submission phase and in the application procedure: general pre-submission advice, specific aspects for intended applications for renewal (notification of intended studies, including their design, public consultation on the intended studies, renewal pre-submission advice by EFSA), notification of information related to studies commissioned or carried out to support an application, public disclosure of non-confidential version of all information submitted in support of the application and related confidentiality decision-making process, public consultation on submitted applications. These new requirements, as implemented by the Practical Arrangements laid down by EFSA, are reflected in this guidance. The guidance describes the procedures and the associated timelines for handling applications related topesticide active substances. Itprovides additional instructionsand guidance to applicants and rapporteur Member States, and co-rapporteur Member Stateswhere relevant, with the aim to enhance the quality of applicationdossiers and assessment reports. The document also provides guidance to applicants and Evaluating Member States on applications for the setting of maximum residue levels, in particular concerning the provisions introduced by the Transparency Regulation amending the General Food Law and their implementation in the procedure for such applications,according to the Practical Arrangements laid down by EFSA.
机译:本文件为提交申请人提交与批准农药活性物质以及制定最大残留水平的申请人的指导,以及成员国在规定范围内提供有关有效物质的评估报告(EC)No 1107/2009和委员会执行监管(欧盟)2020/1740,或关于最大残留水平申请的评估报告,在监管范围内(EC)No 396/2005。它介绍了申请批准,批准或续期农药活性物质的现有批准以及最高残留水平的申请,申请申请,介绍档案的行政要求,以便提交的申请表明2021年3月。它还介绍了在申请(预先提交阶段)的通过和公布EFSA的产出中提供的支助举措。透明度监管通过在提交前阶段和申请程序中引入新规定来修订了一般粮食法:一般预提交咨询,续期申请的具体方面(预期研究通知,包括他们的设计,公众咨询EFSA的预期研究,续期提交建议),与委托或开展的研究有关的信息通知,以支持申请,公开披露在支持申请和相关保密决策的所有信息的所有信息的非机密版本流程,关于提交申请的公开咨询。由EFSA规定的实际安排实施的这些新要求在这一指导下反映出来。该指导描述了处理相关的TOWEMENTIES活性物质的程序和相关时间表。 ITProvides向申请人和报告员成员国的其他指导和指导,以及联合汉堡成员国的国家,旨在提高Applicationsdossiers和评估报告的质量。该文件还为申请人提供指导,并评估成员国关于制定最大残留水平的申请,特别是关于修改一般粮食法的透明度监管的规定及其在此类申请的程序中的执行情况,根据实用EFSA安排安排。

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