Übersetzung für "technical progress " (Englisch → Deutsch) :

Committee for the Adaptation to Technical Progress of the Directives on Dangerous Substances and Preparations | Committee for the Adaptation to Technical Progress of the Directives on Removal of Technical Barriers to Trade in respect of Dangerous Substances and Preparations | Committee on the Adaptation to Technical Progress of the Directives for the Elimination of Technical Barriers to Trade in Dangerous Substances and Preparations

technological change [ adaptation to technical progress | digital revolution | technical progress | technological development | technological progress | Technological innovations(ECLAS) ]

Committee on Adaptation to Technical Progress | Committee on the Adaptation of the Directives to Technical Progress | Technical Progress Committee | CATP [Abbr.] | TPC [Abbr.]

Committee for the adaptation to technical progress of the directives on the removal of technical barriers to trade in colouring matters which may be added to medicinal products | Committee on the adaptation to technical progress of the directives on the elimination of technical barriers to trade in colouring matters which may be added to medicinal products

scrutinise organisational objective progress | test goal progress | analyse goal progress | scrutinise goal progress

assess team's artistic progress | monitor progress in the artistic team | assess artistic team progress | assess progress with the artistic team

tackle an issue that blocks academic progress | tackle issues which block academic progress | provide counseling for issues blocking academic progress | tackle issues that block academic progress

progressive felling by groups | progressive group felling

scientific progress

EUROPA - EU law and publications - EUR-Lex - EUR-Lex - 32014R0133 - EN - Commission Regulation (EU) No 133/2014 of 31 January 2014 amending, for the purposes of adapting to technical progress as regards emission limits, Directive 2007/46/EC of the European Parliament and of the Council, Regulation (EC) No 595/2009 of the European Parliament and of the Council and Commission Regulation (EU) No 582/2011 Text with EEA relevance - COMMISSION REGULATION - (EU) No 133/2014 // of 31 January 2014 // amending, for the purposes of adapting to technical progress as regard ...[+++]s emission limits, Directive 2007/46/EC of the European Parliament and of the Council, Regulation (EC) No 595/2009 of the European Parliament and of the Council and Commission Regulation (EU) No 582/2011 // (Text with EEA relevance) // ‘Appendix 8 // ‘Appendix 6 // Appendix 1

In order to permit adaptation to the technical and scientific progress of Directive 2009/28/EC, the power to adopt acts in accordance with Article 290 TFEU should be delegated to the Commission in respect of possible additions to the list of biofuel feedstocks and fuels, the contribution of which towards the target in Article 3(4) of that Directive should be considered to be twice their energy content, and also in respect of the addition of estimated typical and default values for biofuel and bioliquid pathways, as well as the adaptation of the energy content of transport fuels, as set out in Annex III to Directive 2009/28/EC, to scientific and technical progress.

In order to supplement or amend certain non-essential elements of this Regulation, the power to adopt acts in accordance with Article 290 of the Treaty on the Functioning of the European Union (TFEU) should be delegated to the Commission in respect of: the amendment of Annexes I, II, IV and V to this Regulation in order to adapt them to technical progress or to take account of international regulatory developments in which the Union or the Member States are involved, in the field of clinical trials; the amendment of Annex III in order to improve the information on the safety of medicinal products, to adapt technical requirements to tech ...[+++]nical progress or to take account of international regulatory developments in the field of safety requirements in clinical trials endorsed by bodies in which the Union or the Member States participate; the specification of the principles and guidelines of good manufacturing practice and the detailed arrangements for inspection for ensuring the quality of investigational medicinal products; the amendment of 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.

In order to supplement or amend certain non-essential elements of this Regulation, the power to adopt acts in accordance with Article 290 of the Treaty on the Functioning of the European Union (TFEU) should be delegated to the Commission in respect of: the amendment of Annexes I, II, IV and V to this Regulation in order to adapt them to technical progress or to take account of international regulatory developments in which the Union or the Member States are involved, in the field of clinical trials; the amendment of Annex III in order to improve the information on the safety of medicinal products, to adapt technical requirements to tech ...[+++]nical progress or to take account of international regulatory developments in the field of safety requirements in clinical trials endorsed by bodies in which the Union or the Member States participate; the specification of the principles and guidelines of good manufacturing practice and the detailed arrangements for inspection for ensuring the quality of investigational medicinal products; the amendment of 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.