实施法案层面以下的事实规则制定:欧盟电力市场监管中的双重授权规则制定

IF 1.8 Q1 LAW
Torbjørg Jevnaker, Karianne Krohn Taranger, Per Ove Eikeland, Marie Byskov Lindberg
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引用次数: 0

摘要

在电力市场监管领域,出现了一种做法,即授权链已超越欧盟委员会,造成双重授权。2015-2017 年期间,欧盟委员会通过了实施条例,要求各国能源监管机构共同通过欧洲电力市场和系统运行的详细条款、条件和方法(TCM)。如果后者未能在预定时限内达成一致,则规则制定工作将移交给能源监管机构合作局。这一规则制定程序意味着,根据程序内的动态,不同的行为者将采用《国家电力条例》。本文探讨了双重授权的规则制定是如何在新出现的实践中展开的,如何在实施法案之下演变。通过分析国家机构是否联合采用《中医药法》背后的因素,本研究探讨了这种网络环境下的授权规则制定形式是否能做出决定,或者是否需要由欧盟机构制定规则。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
De Facto Rule-Making Below the Level of Implementing Acts: Double-Delegated Rule-Making in European Union Electricity Market Regulation
Within the area of electricity market regulation, a practice has emerged in which the chain of delegation has gone beyond the European Commission, resulting in double delegation. During 2015–2017, the European Commission adopted implementing regulations requiring detailed European terms, conditions and methodologies (TCMs) for electricity markets and system operation to be jointly adopted by national energy regulators. Should the latter fail to agree within a predefined time limit, rule-making would move to the Agency for the Cooperation of Energy Regulators. This rule-making procedure entails that, depending on the dynamic within the procedure, different actors would adopt the TCMs. This article examines how double-delegated rule-making unfolds in a novel and emerging practice, evolving beneath implementing acts. By analysing the factors behind whether TCMs are adopted jointly by national agencies or not, the study investigates whether this form of delegated rule-making in a network setting delivers decisions or whether rule-making by a European Union agency is needed.
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来源期刊
CiteScore
6.10
自引率
0.00%
发文量
34
期刊介绍: European Journal of Risk Regulation is an interdisciplinary forum bringing together legal practitioners, academics, risk analysts and policymakers in a dialogue on how risks to individuals’ health, safety and the environment are regulated across policy domains globally. The journal’s wide scope encourages exploration of public health, safety and environmental aspects of pharmaceuticals, food and other consumer products alongside a wider interpretation of risk, which includes financial regulation, technology-related risks, natural disasters and terrorism.
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