Examples of Delegated act in a sentence
The Delegated act is based on Article 8(4) of the Taxonomy Regulation.
The Draft Delegated act proposes that SSPEs, for OTC derivatives in connection with securitisations that meet the requirements to be classified as securitisations according to the Securitisation Regulation, would be exempted from posting and collecting initial margins and from posting variation margins in the way already implemented for covered bonds.
That Directive will be repealed by Regulation (EU) No 167/2013 with effect from 1 January 2016 and therefore its provisions must be carried over to this Delegated act.
The meeting brought together experts, at EU and national levels, including public authorities, associations, training institutions and EU stakeholders, to discuss this topic.This is an ongoing topic, that the EFN will follow closely in 2020, and for which it is key the EFN and its members lobby for, promoting the EFN proposed Delegated act, as agreed with the nursing regulators network (2016).
Indeed, the process and requirements to obtain cross-border waivers under Article 8 of CRR, or exemption of the cap of intragroup inflows under Article 33 of LCR Delegated act is very burdensome.
According to Annex II f) of the ITS Directive, the Delegated act shall “Respect coherence-take into account existing Union rules, policies and activities which are relevant in the field of ITS, in particular in the field of standardisation”.
A draft Commission Delegated act was discussed in February 2020 and May 2020.In accordance with the Better Regulation agenda, the draft Commission Delegated act was open for feedback for a period of four weeks4.
Three of them were not related to this Delegated act, but to the Delegated Act amending Regulation (EU) No 639/20141 .
Or. en Justification The Commission should accordingly be empowered to adopt by Delegated act a list ofcountries to which exports are prohibited.
Delegated act The Commission shall be empowered to adopt delegated acts in accordance with Article 89 in respect of amending Annex VI in order to ensure subject safety and the reliability and robustness of data generated in a clinical trial or to take account of technical progress.