Примери за използване на Amend or withdraw на Английски и техните преводи на Български
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After such a review the Commission may decide to maintain, amend or withdraw the proposal.
Amend or withdraw its draft measure, taking utmost account of the European Commission's notification referred to in paragraph 1 and of BEREC's opinion and cooperation;
The Commission is then obliged to review its proposed act in the light of this input anddecide whether to maintain, amend or withdraw it.
The national regulatory authority may impose, amend or withdraw specific obligations in accordance with Article 6(2) of Directive 2002/20/EC(Authorisation Directive).';
After the'yellow card' review,the authoring institution(usually the Commission) may decide to maintain, amend or withdraw the legislation.
Хората също превеждат
On the basis of its assessment, the national regulatory authority shall impose,maintain, amend or withdraw obligations, in accordance with Articles 6 and 7 of Directive 2002/21/EC(Framework Directive).
The national regulatory authority concerned should undertake a new analysis of the markets in which the segregated entity operates, and impose,maintain, amend or withdraw obligations accordingly.
Amend or withdraw the draft decisionor the set of planned measures, taking utmost account of the European Commission's notification and of BEREC's opinion and recommendations referred to in Paragraph one of this Section; or. .
EU countries' authorities may refuse to grant an export authorisation and cancel,suspend, amend or withdraw an authorisation that has already been granted.
If the reasoned opinions submitted correspond to at least one third of the votes, the Commission has to review its proposal andmay decide to maintain, amend or withdraw it.
In the case of a product containing cyflufenamid as the only active substance,where necessary, amend or withdraw the authorisation by 30 September 2011 at the latest; or. .
There will be a reinforced control mechanism of subsidiarity in the sense that if a draft legislative act is contested by a simple majority of the votes allocated to national parliaments, the Commission will re-examine the draft act,which it may decide to maintain, amend or withdraw.
In the case of a product containing cyflufenamid as the only active substance,where necessary, amend or withdraw the authorisation by 30 September 2011 at the latest; or. .
At its own discretion the Communications Regulation Commission may impose,maintain, amend or withdraw specific obligations on undertakings with SMP on a relevant market to provide efficient access, interconnection(or both) and interoperability of services in order to benefit end-users and encourage effective competition.
In the case of a product containing aclonifen, imidacloprid and metazachlor as the only active substance,where necessary, amend or withdraw the authorisation by 31 January 2014 at the latest; or. .
Member States shall in accordance with Directive 91/414/EEC, where necessary, amend or withdraw existing authorisations for plant protection products containing aclonifen, imidacloprid and metazachlor as active substances by 31 January 2010.
In the case of a product containing aclonifen, imidacloprid and metazachlor as the only active substance,where necessary, amend or withdraw the authorisation by 31 January 2014 at the latest; or. .
Member States shall in accordance with Directive 91/414/EEC, where necessary, amend or withdraw existing authorisations for plant protection products containing dimethoate, dimethomorph, glufosinate, metribuzin, phosmet and propamocarb as active substances by 31 March 2008.
In the case of a product containing aclonifen, imidacloprid andmetazachlor as the only active substance, where necessary, amend or withdraw the authorisation by 31 January 2014 at the latest; or. .
On the basis of its assessment, the national regulatory authority shall impose,maintain, amend or withdraw obligations, in accordance with Articles 236 and 32 7 of Directive 2002/21/EC(Framework Directive), ð applying, if appropriate.
If a third of them find the draft legislation does not comply with the subsidiarity principle, the Commission has to review the proposal anddecide whether to keep, amend or withdraw it and to justify its decision.
Member States shall in accordance with Directive 91/414/EEC,where necessary, amend or withdraw existing authorisations for plant protection products containing tetraconazole as an active substance by 30 June 2010.
If a third of them find the draft legislation does not comply with the subsidiarity principle, the Commission has to review the proposal anddecide whether to keep, amend or withdraw it and to justify its decision.
Member States shall in accordance with Directive 91/414/EEC, where necessary, amend or withdraw existing authorisations for plant protection products containing tetraconazole as an active substance by 30 June 2010.
If the Regulator receives the opinion from the European Commission regarding the draft decision,it shall, within six months from the day of taking of the decision of the European Commission, amend or withdraw the draft decision in accordance with this opinion.
In relation to the third indent of the firstsubparagraph of paragraph 3, national regulatory authorities shall notify decisions to impose, amend or withdraw obligations on market players to the Commission, in accordance with the procedure referred to in Article 7 of Directive 2002/21/EC(Framework Directive).
In such a case, the Commission shall review the draft implementing act, taking account of the positions expressed, and shall inform the European Parliament andthe Council whether it intends to maintain, amend or withdraw the draft implementing act.
Where, as a result of this market analysis, a national regulatory authority finds that one or more operators do not have significant market power on the relevant market,it may amend or withdraw the conditions with respect to those operators, in accordance with the procedures referred to in Articles 23 and 32, only to the extent that.
In such instances, the Commission will review the draft implementing act, taking account of the positions expressed, and will inform the European Parliament andthe Council of the EU whether it intends to maintain, amend or withdraw the draft implementing act.
In the case of a product containing dimethoate, dimethomorph, glufosinate, metribuzin, phosmet and propamocarb as the only active substance,where necessary, amend or withdraw the authorisation by 30 September 2011 at the latest; or. .