natgillin/translations-raw huggingface dataset:
Directive 2001/13/EC of the European Parliament and of the Council of 26 February 20013, which amended a pre-existing Council Directive of 27 June 1995 on the licensing of railway undertakings4; and
Direktiva Evropskega parlamenta in Sveta 2001/13/ES z dne 26. februarja 20013, ki je spremenila že obstoječo Direktivo Sveta z dne 27. junija 1995 o izdaji licence prevoznikom v železniškem prometu4; ter
Directive 2001/14/EC of the European Parliament and of the Council 26 February 2001 on the allocation of railway infrastructure capacity and the levying of charges for the use of railway infrastructure and safety certification
Direktiva Evropskega parlamenta in Sveta 2001/14/ES z dne 26. februarja 2001 o dodeljevanju železniških infrastrukturnih zmogljivosti, naložitvi uporabnin za uporabo železniške infrastrukture in podeljevanju varnostnega spričevala
Directive 2001/14/EC of the European Parliament and of the Council of 26 February 2001 on the allocation of railway infrastructure capacity and the levying of charges for the use of railway infrastructure5.
Direktiva Evropskega parlamenta in Sveta 2001/14/ES z dne 26. februarja 2001 o dodeljevanju železniških infrastrukturnih zmogljivosti, naložitvi uporabnin za uporabo železniške infrastrukture in podeljevanju varnostnega spričevala5.
DIRECTIVE 2001/16/EC OF THE EUROPEAN PARLIAMENT AND OF THE COUNCIL
DIREKTIVA 2001/16/ES EVROPSKEGA PARLAMENTA IN SVETA
Directive 2001/18/EC is amended as follows:
Direktiva 2001/18/ES se spremeni:
Directive 2001/18/EC of the European Parliament and of the Council of 12 March 2001 on the deliberate release into the environment of genetically modified organisms and repealing Council Directive 90/220/EEC15 and Regulation (EC) No 1829/2003 of the European Parliament and of the Council of 22 September 2003 on genetically modified food and feed16 establish a comprehensive legal framework for the authorisation of genetically modified organisms (GMOs), which is fully applicable to GMOs to be used for cultivation purposes throughout the EU as seeds or other plant-propagating material (hereinafter 'GMOs for cultivation').
Direktiva 2001/18/ES Evropskega parlamenta in Sveta z dne 12. marca 2001 o namernem sproščanju gensko spremenjenih organizmov v okolje in razveljavitvi Direktive Sveta 90/220/EGS15 ter Uredba (ES) št. 1829/2003 Evropskega parlamenta in Sveta z dne 22. septembra 2003 o gensko spremenjenih živilih in krmi16 vzpostavljata celovit pravni okvir za odobritev gensko spremenjenih organizmov (GSO), ki se v celoti uporablja za GSO, ki se po vsej EU uporabljajo za gojenje v obliki semen ali drugega razmnoževalnega materiala rastlin (v nadaljnjem besedilu: GSO za gojenje).
Directive 2001/18/EC of the European Parliament and of the Council5 provides that certain measures are to be adopted in accordance with Council Decision 1999/468/EC of 28 June 1999 laying down the procedures for the exercise of implementing powers conferred on the Commission6.
Direktiva 2001/18/ES Evropskega parlamenta in Sveta5 določa, da je treba sprejeti nekatere ukrepe v skladu s Sklepom Sveta 1999/468/ES z dne 28. junija 1999 o določitvi postopkov za uresničevanje Komisiji podeljenih izvedbenih pooblastil6.
Directive 2001/18/EC, should therefore be amended accordingly,
Direktivo 2001/18/ES je zato treba ustrezno spremeniti
Directive 2001/20/EC
Direktiva 2001/20/ES
Directive 2001/20/EC aimed to simplify and harmonise the administrative provisions governing clinical trials in the European Union.
Cilj Direktive 2001/20/ES sta bili poenostavitev in uskladitev upravnih določb, ki urejajo klinična preskušanja v Evropski uniji.
Directive 2001/20/EC contained an extensive set of rules for the protection of subjects.
Direktiva 2001/20/ES vključuje obsežen sklop pravil za zaščito udeležencev.
Directive 2001/20/EC contains relatively few rules on the actual conduct of trials.
Direktiva 2001/20/ES vključuje razmeroma malo pravil o dejanskem izvajanju preskušanj.
Directive 2001/20/EC had already referred to this database and to the European Medicines Agency's role in administering it.
Že Direktiva 2001/20/ES se sklicuje na to podatkovno zbirko in na vlogo Evropske agencije za zdravila pri njenem upravljanju.
Directive 2001/20/EC has brought about important improvements in the safety and ethical soundness of clinical trials in the EU and in the reliability of clinical trials data.
Direktiva 2001/20/ES je uvedla pomembne izboljšave glede varnosti in etične neoporečnosti kliničnih preskušanj v EU ter glede zanesljivosti podatkov iz kliničnih preskušanj.
Directive 2001/20/EC introduced an 'obligatory insurance/indemnity'.
Direktiva 2001/20/ES je uvedla „obvezno zavarovanje/odškodninski mehanizem“.
Directive 2001/20/EC is repealed as of [please set a specific date - two years after publication of this Regulation].
Direktiva 2001/20/ES se razveljavi [navesti datum – dve leti po objavi te uredbe].
Directive 2001/20/EC of the European Parliament and of the Council of 4 April 2001 on the approximation of the laws, regulations and administrative provisions of the Member States relating to the implementation of good clinical practice in the conduct of clinical trials on medicinal products for human use – Page 14.
Direktiva 2001/20/ES Evropskega parlamenta in Sveta z dne 4. aprila 2001 o približevanju zakonov in drugih predpisov držav članic v zvezi z izvajanjem dobre klinične prakse pri kliničnem preskušanju zdravil za ljudi – stran 14.
Directive 2001/20/EC of the European Parliament and of the Council of 4 April 2001 on the approximation of the laws, regulations and administrative provisions of the Member States relating to the implementation of good clinical practice in the conduct of clinical trials on medicinal products for human use53;
Direktivo 2001/20/ES Evropskega parlamenta in Sveta z dne 4. aprila 2001 o približevanju zakonov in drugih predpisov držav članic v zvezi z izvajanjem dobre klinične prakse pri kliničnem preskušanju zdravil za ljudi53;
Directive 2001/20/EC of the European Parliament and of the Council of 4 April 2001,
5.7. Direktiva 2001/20/ES Evropskega Parlamenta in Sveta z dne 4. aprila 2001
Directive 2001/20/EC should be repealed to ensure that only one set of rules applies to the conduct of clinical trials in the Union.
Direktivo 2001/20/ES bi bilo treba razveljaviti, da se zagotovi uporaba samo enega sklopa pravil za izvajanje kliničnih preskušanj v Uniji.
Directive 2001/20/EC1 has brought about important improvements in the safety and ethical soundness of clinical trials in the EU and in the reliability of clinical trials data.
Direktiva 2001/20/ES1 je uvedla pomembne izboljšave glede varnosti in etične neoporečnosti kliničnih preskušanj v EU ter glede zanesljivosti podatkov iz kliničnih preskušanj.
Directive 2001/24/EC is amended as follows:
Direktiva 2001/24/ES se spremeni:
Directive 2001/25/EC , as amended by the Directives listed in Annex III, Part A, is repealed, without prejudice to the obligations of the Member States relating to the time limits for transposition into national law of the Directives set out in Annex III, Part B.
Direktiva 2001/25/ES, kakor je bila spremenjena z direktivami navedenimi v Prilogi III, Del A, je razveljavljena, brez poseganja v obveznosti držav članic glede rokov za prenos v nacionalno zakonodajo direktiv, ki so navedeni v Prilogi III, Del B.
Directive 2001/29/EC of 22 May 200111 on the harmonisation of certain aspects of copyright and related rights in the information society supplemented the protection afforded by Directive 98/84/EC three years after the adoption of the latter.
Direktiva 2001/29/ES z dne 22. maja 200111 o avtorskih pravicah v informacijski družbi je dopolnila varstvo, zagotovljeno z Direktivo 98/84/ES, tri leta po sprejetju slednje direktive.
Directive 2001/29/EC of the European Parliament and of the Council of 22 May 2001 on the harmonisation of certain aspects of copyright and related rights in the information society20 requires a licence for each of the rights in the online exploitation of musical works.
V skladu z Direktivo 2001/29/ES Evropskega parlamenta in Sveta z dne 22. maja 2001 o usklajevanju določenih vidikov avtorske in sorodnih pravic v informacijski družbi20 se za vsako pravico pri spletnem izkoriščanju glasbenih del zahteva licenca.
Directive 2001/37/EC of the European Parliament and of the Council of 5 June 2001 on the approximation of the laws, regulations and administrative provisions of the Member States concerning the manufacture, presentation and sale of tobacco products – Page 64.
Direktiva 2001/37/ES Evropskega parlamenta in Sveta z dne 5. junija 2001 o približevanju zakonov in drugih predpisov držav članic o izdelavi, predstavitvi in prodaji tobačnih izdelkov – stran 59.
Directive 2001/37/EC of the European Parliament and of the Council on the approximation of the laws, regulations and administrative provisions of the Member States concerning the manufacture, presentation and sale of tobacco products (Tobacco Products Directive, hereafter TPD) was adopted on 5 June 2001.1 More than ten years have passed since the adoption and it has become necessary to consider and examine options to update the TPD in line with market, scientific and international developments, in particular the WHO Convention on Tobacco Control (FCTC) to which the European Union and all the Member States are Party.
Direktiva 2001/37/ES Evropskega parlamenta in Sveta o približevanju zakonov in drugih predpisov držav članic o izdelavi, predstavitvi in prodaji tobačnih izdelkov (direktiva o tobačnih izdelkih, v nadaljnjem besedilu: DTI) je bila sprejeta 5. junija 20011. Od sprejetja je minilo več kot deset let in preučiti je treba možnosti za posodobitev DTI, da bo odražala tržni, znanstveni in mednarodni razvoj, zlasti Okvirno konvencijo Svetovne zdravstvene organizacije za nadzor nad tobakom (v nadaljnjem besedilu: Okvirna konvencija).
Directive 2001/42/EC1 on the assessment of the effects of certain plans and programmes on the environment (‘Strategic Environmental Assessment’ – hereinafter the 'SEA – Directive') requires certain public plans and programmes (P &amp; P) to undergo an environmental assessment before they are adopted.
Direktiva 2001/42/ES1 o presoji vplivov nekaterih načrtov in programov na okolje (v nadaljnjem besedilu: Direktiva o strateški okoljski presoji, Direktiva SOP) zahteva, da se za nekatere javne načrte in programe izvede okoljska presoja, preden se sprejmejo.
Directive 2001/43/EC of the European Parliament and of the Council of 27 June 2001 amending Council Directive 92/23/EEC relating to tyres for motor vehicles and their trailers and to their fitting
Direktiva 2001/43/ES Evropskega parlamenta in Sveta z dne 27. junija 2001 o spremembah Direktive Sveta 92/23/EGS o pnevmatikah za motorna in priklopna vozila ter o njihovi vgradnji
Directive 2001/43/EC of the European Parliament and of the Council of 27 June 2001 amending Council Directive 92/23/EEC5.
Direktiva Evropskega parlamenta in Sveta 2001/43/ES z dne 27. junija 2001 o spremembi Direktive Sveta 92/23/EGS5.
Directive 2001/46/EC of the European Parliament and of the Council of 23 July 2001 amending Council Directive 95/53/EC and Council Directives 70/524/EEC, 96/25/EC and 1999/29/EC12.
Direktiva Evropskega parlamenta in Sveta 2001/46/ES z dne 23. julija 2001 o spremembi Direktive Sveta 95/53/ES in direktiv Sveta 70/524/EGS, 96/25/ES in 1999/29/ES12.
Directive 2001/46/EC of the European Parliament and of the Council of 23 July 2001 amending Council Directive 95/53/EC fixing the principles governing the organisation of official inspections in the field of animal nutrition and Council Directives 70/524/EEC, 96/25/EC and 1999/29/EC on animal nutrition
Direktiva Evropskega parlamenta in Sveta 2001/46/ES z dne 23. julija 2001 o spremembi Direktive Sveta 95/53/ES o določitvi načel, ki urejajo organizacijo uradnega nadzora na področju prehrane živali, in direktiv 70/524/EGS, 96/25/ES in 1999/29/ES o prehrani živali
Directive 2001/56/EC of the European Parliament and of the Council of 27 September 2001 relating to heating systems for motor vehicles and their trailers, amending Council Directive 70/156/EEC and repealing Council Directive 78/548/EEC61,
Direktivo 2001/56/ES Evropskega parlamenta in Sveta z dne 27. septembra 2001 o ogrevalnih sistemih motornih in priklopnih vozil, ki spreminja Direktivo Sveta 70/156/EGS in razveljavlja Direktivo Sveta 78/548/EGS61,
Directive 2001/77/EC of the European Parliament and of the Council of 27 September 2001 on the promotion of electricity produced from renewable energy sources in the internal electricity market5 and Directive 2003/30/EC of the European Parliament and of the Council of 8 May 2003 on the promotion of the use of biofuels or other renewable fuels for transport6 established definitions for different types of renewable energy.
V Direktivi 2001/77/ES Evropskega parlamenta in Sveta z dne 27. septembra 2001 o spodbujanju proizvodnje električne energije iz obnovljivih virov energije na notranjem trgu5 in Direktivi 2003/30/ES Evropskega parlamenta in Sveta z dne 8. maja 2003 o pospeševanju rabe biogoriv in drugih obnovljivih goriv v sektorju prevoza6 so določene opredelitve za različne vrste obnovljive energije.
Directive 2001/80/EC of the European Parliament and of the Council of 23 October 2001 on the limitation of emissions of certain pollutants into the air from large combustion plants;
Direktive 2001/80/ES Evropskega parlamenta in Sveta z dne 23. oktobra 2001 o omejevanju emisij nekaterih onesnaževal v zrak iz velikih kurilnih naprav;
Directive 2001/80/EC of the European Parliament and of the Council of 23 October 2001 on the limitation of emissions of certain pollutants into the air from large combustion plants
Direktova 2001/80/ES Evropskega parlamenta in Sveta z dne 23. oktobra 2001 o omejevanju emisij nekaterih onesnaževal v zrak iz velikih kurilnih naprav
Directive 2001/81/EC of the European Parliament and of the Council of 23 October 2001 on national emission ceilings for certain atmospheric pollutants21
Direktiva 2001/81/ES Evropskega parlamenta in Sveta z dne 23. oktobra 2001 o nacionalnih zgornjih mejah emisij za nekatera onesnaževala zraka21
Directive 2001/81/EC of the European Parliament and of the Council of 23 October 2001 on national emission ceilings for certain atmospheric pollutants;
Direktive 2001/81/ES Evropskega parlamenta in Sveta z dne 23. oktobra 2001 o nacionalnih zgornjih mejah emisij za nekatera onesnaževala zraka;
Directive 2001/81/EC of the European Parliament and of the Council1 set annual national emission ceilings for each Member State to be attained by 2010, covering emissions of sulphur dioxide (SO2), nitrogen oxides (NOx), non-methane volatile organic compounds (NMVOC) and ammonia (NH3).
Direktiva 2001/81/ES Evropskega parlamenta in Sveta1 je določila letne nacionalne zgornje meje emisij, ki jih mora vsaka država članica doseči do leta 2010, veljajo pa za emisije žveplovega dioksida (SO2), dušikove okside (NOx), nemetanske hlapne organske spojine (NMHOS) in amoniak (NH3).
Directive 2001/82/EC and Regulation (EC) No 726/2004 are based on Articles 95 and 152 (4)(b) of the Treaty establishing the European Community respectively.
Direktiva 2001/82/ES in Uredba (ES) št. 726/2004 temeljita na členu 95 oz. členu 152(4)(b) Pogodbe o ustanovitvi Evropske skupnosti.
Directive 2001/82/EC and Regulation (EC) No 726/2004 provide the legal environment on the manufacture, authorisation, marketing, distribution and use of veterinary medicines.
Direktiva 2001/82/ES in Uredba (ES) št. 726/2004 zagotavljata pravno okolje za proizvodnjo, izdajo dovoljenj, dajanje v promet, distribucijo in uporabo zdravil za uporabo v veterinarski medicini.
Directive 2001/82/EC of the European Parliament and of the Council of 6 November 2001 on the Community code relating to veterinary medicinal products – Page 16.
Direktiva 2001/82/ES Evropskega parlamenta in Sveta z dne 6. novembra 2001 o zakoniku Skupnosti o zdravilih za uporabo v veterinarski medicini – stran 15.
Directive 2001/82/EC of the European Parliament and of the Council of 6 November 2001,
5.8. Direktiva 2001/82/ES Evropskega Parlamenta in Sveta z dne 6. novembra 2001
Directive 2001/82/EC of the European Parliament and of the Council11 and Regulation (EC) No 726/2004 of the European Parliament and of the Council12 constitute the Union regulatory framework for the placing on the market, manufacture, import, export, supply, pharmacovigilance, control and the use of veterinary medicinal products.
Direktiva 2001/82/ES Evropskega parlamenta in Sveta11 ter Uredba (ES) št. 726/2004 Evropskega parlamenta in Sveta12 tvorita regulativni okvir Unije za dajanje v promet, proizvodnjo, uvoz, izvoz, dobavo, farmakovigilanco, nadzor in uporabo zdravil za uporabo v veterinarski medicini.
Directive 2001/82/EC of the European Parliament and of the Council5 and Regulation (EC) 726/2004 of the European Parliament and of the Council6 constituted the Union regulatory framework for the manufacture, authorisation and distribution of veterinary medicinal products.
Direktiva 2001/82/ES Evropskega parlamenta in Sveta5 ter Uredba (ES) št. 726/2004 Evropskega parlamenta in Sveta6 sta bila regulativni okvir Unije za proizvodnjo zdravil za uporabo v veterinarski medicini, izdajo dovoljenj za njihovo uporabo ter za distribucijo teh zdravil.
Directive 2001/83/EC does not prevent Member States from establishing their own approaches regarding the provisions on information on medicinal products.
Direktiva 2001/83/ES državam članicam ne preprečuje, da uvedejo svoje pristope k določbam glede informacij o zdravilih.
Directive 2001/83/EC of the European Parliament and of the Council of 6 November 2001 on the Community code relating to medicinal products for human use11 lays down harmonised rules for the authorisation, supervision and pharmacovigilance of medicinal products within the Community.
Direktiva 2001/83/ES Evropskega parlamenta in Sveta z dne 6. novembra 2001 o zakoniku Skupnosti o zdravilih za uporabo v humani medicini11 določa usklajena pravila za pridobitev dovoljenja za promet z zdravilom in nadzor in farmakovigilanco zdravil znotraj Skupnosti.
Directive 2001/83/EC of the European Parliament and of the Council of 6 November 2001 on the Community code relating to medicinal products for human use2, as regards general rules on medicinal products for human use and specific rules for medicinal products authorised by the Member States.
Direktivi 2001/83/ES Evropskega parlamenta in Sveta z dne 6. novembra 2001 o zakoniku Skupnosti o zdravilih za uporabo v humani medicini2 glede splošnih pravil za zdravila za uporabo v humani medicini in posebnih pravil za zdravila, za katera dovoljenja izdajo države članice.
Directive 2001/83/EC of the European Parliament and of the Council of 6 November 2001 on the Community code relating to medicinal products for human use2, as regards general rules on medicinal products for human use and specific rules for medicinal products authorised by the Member States.
Direktivi 2001/83/ES Evropskega parlamenta in Sveta z dne 6. novembra 2001 o zakoniku Skupnosti o zdravilih za uporabo v humani medicini2, kar zadeva splošna pravila o zdravilih za humano uporabo in posebna pravila za zdravila, ki jih odobrijo države članice.
Directive 2001/83/EC of the European Parliament and of the Council of 6 November 2001 on the Community code relating to medicinal products for human use4 establishes harmonised rules on the advertising of medicinal products for human use.
Direktiva 2001/83/ES Evropskega parlamenta in Sveta z dne 6. novembra 2001 o zakoniku Skupnosti o zdravilih za uporabo v humani medicini4 določa usklajena pravila o oglaševanju zdravil za uporabo v humani medicini.
Directive 2001/83/EC of the European Parliament and of the Council of 6 November 2001 on the Community code relating to medicinal products for human use5 establishes harmonised rules on the advertising of medicinal products for human use.
Direktiva 2001/83/ES Evropskega parlamenta in Sveta z dne 6. novembra 2001 o zakoniku Skupnosti o zdravilih za uporabo v humani medicini5 določa usklajena pravila o oglaševanju zdravil za uporabo v humani medicini.
Directive 2001/86/EC of 8 October 2001 supplementing the Statute for a European company with regard to the involvement of employees;
Direktiva 2001/86/ES z dne 8. oktobra 2001 o dopolnitvi Statuta evropske družbe glede udeležbe delavcev;
Directive 2001/95/EC of the European Parliament and of the Council of 3 December 2001 on general product safety – Page 66.
Direktiva 2001/95/ES Evropskega parlamenta in Sveta z dne 3. decembra 2001 o splošni varnosti proizvodov – stran 61.
Directive 2001/96/EC of the European Parliament and of the Council Directive of 4 December 2001 establishing harmonised requirements and procedures for the safe loading and unloading of bulk carriers
Direktiva 2001/96/ES Evropskega parlamenta in Sveta z dne 4. decembra 2001 o določitvi usklajenih zahtev in postopkov za varno nakladanje in razkladanje ladij za prevoz razsutega tovora
Directive 2001/96/EC of the European Parliament and of the Council Directive of 4 December 2001 establishing harmonised requirements and procedures for the safe loading and unloading of bulk carriers57
Direktiva 2001/96/ES Evropskega parlamenta in Sveta z dne 4. decembra 2001 o določitvi usklajenih zahtev in postopkov za varno nakladanje in razkladanje ladij za prevoz razsutega tovora57
Directive 2002/14/EC of 11 March 2002 establishing a general framework for informing and consulting employees in the European Community
Direktive 2002/14/ES z dne 11. marca 2002 o določitvi splošnega okvira za obveščanje in posvetovanje z delavci v Evropski skupnosti,
Directive 2002/14/EC of the European Parliament and of the Council of 11 March 2002 establishing a general framework for informing and consulting employees in the European Community6 lays down the general principles to be applied at national level.
Direktiva 2002/14/ES Evropskega parlamenta in Sveta z dne 11. marca 2002 o določitvi splošnega okvira za obveščanje in posvetovanje z delavci v Evropski skupnosti6 določa splošna načela uporabe na nacionalni ravni.
Directive 2002/15/EC establishes minimum requirements in relation to the organisation of working time in order to improve the health and safety protection of persons performing mobile road transport activities, to improve road safety and to align conditions of competition.
Direktiva 2002/15/ES določa minimalne zahteve v zvezi z urejanjem delovnega časa za izboljšanje zdravja in varnosti oseb, ki opravljajo spremljevalne dejavnosti v cestnem prometu, povečanje varnosti v cestnem prometu in uskladitev konkurenčnih pogojev.
Directive 2002/21/EC of the European Parliament and of the Council of 7 March 2002 on a common regulatory framework for electronic communications networks and services as amended by Directive 2009/140/EC of the European Parliament and of the Council of 25 November 2009
Direktiva evropskega parlamenta in sveta 2002/21/ES z dne 7. marca 2002 o skupnem regulativnem okviru za elektronska komunikacijska omrežja in storitve, kakor je bila spremenjena z Direktivo 2009/140/ES Evropskega parlamenta in Sveta z dne 25. novembra 2009