qanastek/ELRC-Medical-V2 huggingface dataset:
English: Therefore, further technical progress needs to be reported before proceeding with the preparation of a delegated act in relation to new means of identification of bovine animals;
Translation (en-mt): Għalhekk, irid jiġi rrappurtat aktar progress tekniku qabel ma wieħed jipproċedi bit-tħejjija ta' att delegat dwar mezzi ġodda ta' identifikazzjoni tal-annimali bovini;
English: [4: Commission Regulation (EC) No 644/2005 of 27 April 2005 authorising a special identification system for bovine animals kept for cultural and historical purposes on approved premises as provided for in Regulation (EC) No 1760/2000 of the European Parliament and of the Council (OJ L 107, 28.4.2005, p.
Translation (en-mt): Ir-Regolament tal-Kummissjoni (KE) Nru 644/2005 tas-27 ta' April 2005 li jawtorizza sistema ta' identifikazzjoni speċifika għall-annimali bovini miżmuma għal għanijiet kulturali u storiċi f'postijiet approvati kif previst fir-Regolament (KE) Nru 1760/2000 tal-Parlament Ewropew u tal-Kunsill (ĠU L 107, 28.4.2005, p. 18).]
English: So far, the Commission has supplemented the requirements of the Bovine Identification Regulation concerning matters referred to in Articles 4(3), 4(5), 7(1), 7(6), 13(6) and 14 of that Regulation.
Translation (en-mt): Sa issa, il-Kummissjoni ssupplimentat ir-rekwiżiti tar-Regolament dwar l-Identifikazzjoni tal-Bhejjem tal-Fart f'dak li għandu x'jaqsam mal-kwistjonijiet imsemmija fl-Artikoli 4(3), 4(5), 7(1), 7(6), 13(6) u 14 ta' dak ir-Regolament.
English: The Commission does at this stage not consider to proceed with the preparation of delegated acts in relation to any of the delegated powers referred to in Articles 4(1), 4a(2), 5, 6(2) or 7(2) of the Bovine Identification Regulation since this Regulation is to be amended by Regulation (EU) 2016/4293 by deleting Articles 1 to 10 as from 21 April 2021.
Translation (en-mt): F'dan l-istadju l-Kummissjoni mhijiex taħseb biex tipproċedi bit-tħejjija ta' xi atti delegati rigward xi waħda mis-setgħat delegati msemmijin fl-Artikoli 4(1), 4a(2), 5, 6(2) jew 7(2) tar-Regolament dwar l-Identifikazzjoni tal-Bhejjem tal-Fart billi dan ir-Regolament se jiġi emendat bir-Regolament (UE) 2016/4293 billi jitħassru l-Artikoli 1 sa 10 mill-21 ta' April 2021.
English: [8: Commission Decision 2001/672/EC of 20 August 2001 laying down special rules applicable to movements of bovine animals when put out to summer grazing in mountain areas (OJ L 235, 4.9.2001, p.
Translation (en-mt): Id-Deċiżjoni tal-Kummissjoni 2001/672/KE tal-20 ta' Awwissu 2001 li tistabbilixxi regoli speċjali applikabbli għall-movimenti ta' annimali bovini meta mqegħda jirgħu fis-sajf fl-oqsma tal-muntanji (ĠU L 235, 4.9.2001, p. 23).]
English: Treatment data:
Translation (en-mt): Id-data tat-trattamenti:
English: Period: 1/1/2016 - 31/12/2017
Translation (en-mt): Perjodu: 01/01/2016 - 31/12/2017
English: [2: OJ L 66, 13.3.1999, p. 24][3: OJ C 283, 24.11.2009, p. 5]
Translation (en-mt): [2: ĠU L 66, 13.3.1999, p. 24.][3: ĠU C 283, 24.11.2009, p. 5.]
English: [4: OJ C 37, 30.1.2019, p. 6]
Translation (en-mt): ĠU C 37, 30.1.2019, p. 6.]
English: Number of samples analysed: 11 162
Translation (en-mt): L-għadd ta' kampjuni analizzati: 11 162
English: [1: OJ L 66, 13.3.1999, p.
Translation (en-mt): [1: ĠU L 66, 13.3.1999, p. 16.]
English: Source: 28 Member States and Norway
Translation (en-mt): Sors: 28 Stat Membru u n-Norveġja
English: Five countries (four Member States and Norway) did not perform any analytical checks at product marketing stage in 2016-2017 due to budgetary restrictions (Croatia (2016), Denmark (2017) and Norway (2016 and 2017)), lack of laboratory capacity (Estonia and Cyprus (2016, 2017)) or other control priorities (Sweden (2016, 2017)).
Translation (en-mt): Ħames pajjiżi (erba' Stati Membri u n-Norveġja) ma wettqu l-ebda kontrolli analitiċi fl-istadju tal-kummerċjalizzazzjoni tal-prodott fl-2016-2017 minħabba restrizzjonijiet baġitarji (il-Kroazja (2016), id-Danimarka (2017) u n-Norveġja (2016 u 2017)), in-nuqqas ta' kapaċità tal-laboratorji (l-Estonja u Ċipru (2016, 2017) jew prijoritajiet oħra ta' kontroll (l-Iżvezja (2016, 2017).
English: Main place of irradiation: Belgium (68%) and the Netherlands (13%)
Translation (en-mt): Il-Belġju (68 %) u n-Netherlands (13 %)
English: There are now 24 irradiation facilities in the EU.
Translation (en-mt): Issa hemm 24 faċilità ta' irradjazzjoni fl-UE.
English: From the total of 11 162 samples, 87 were not compliant (0.8%) and 113 samples (1%) gave inconclusive results.
Translation (en-mt): Minn total ta' 11 162 kampjun, 87 ma kinux konformi (0,8 %) u 113 kampjun (1 %) ma wasslux għal riżultati konklużivi.
English: Approved irradiation facilities
Translation (en-mt): Faċilitajiet approvati ta' irradjazzjoni
English: Radiant energy has differing wavelengths and degrees of power and disappears when the energy source is removed.
Translation (en-mt): L-enerġija radjanti għandha tul ta' mewġ u gradi ta' potenza differenti u tisparixxi meta jitneħħa s-sors tal-enerġija.
English: Quantity of products treated: 10 211 tonnes (-11.4%) compared to 2015 on average
Translation (en-mt): Il-kwantità ta' prodotti ttrattati: 10 211 tunnellata (-11,4%) meta mqabbel mal-2015, bħala medja
English: The facilities are located in 14 Member States: five in France, four in Germany, two in Bulgaria, the Netherlands, and Spain, one in Belgium, Czech Republic, Croatia, Estonia, Italy, Hungary, Poland, Romania and United Kingdom.
Translation (en-mt): Il-faċilitajiet jinsabu f'14-il Stat Membru: ħamsa fi Franza, erbgħa fil-Ġermanja, tnejn fil-Bulgarija, fin-Netherlands u fi Spanja, u waħda fil-Belġju, fir-Repubblika Ċeka, fil-Kroazja, fl-Estonja, fl-Italja, fl-Ungerija, fil-Polonja, fir-Rumanija u fir-Renju Unit.
English: A total quantity of 10 211 tonnes of products were treated with ionising irradiation in EU Member States during the years 2016 and 2017.
Translation (en-mt): Kwantità totali ta' 10 211 tunnellata ta' prodotti ġew trattati bl-irradjazzjoni jonizzanti fl-Istati Membri tal-UE waqt is-snin 2016 u 2017.
English: Number of approved facilities: 24
Translation (en-mt): L-għadd ta' faċilitajiet approvati: 24
English: For the period 2016-2017, 11 162 samples were analysed by 24 Member States, i.e. overall 7.02% less in average than in 2015.
Translation (en-mt): Għall-perjodu 2016-2017, 11 162 kampjun ġew analizzati minn 24-il Stat Membru, jiġifieri b'mod ġenerali 7,02 % inqas mill-medja fl-2015.
English: Cereals, seed, vegetables, fruits and their
Translation (en-mt): Ċereali, żrieragħ, ħxejjex, frott u
English: vegetables seasoning(20.77%)
Translation (en-mt): ħwawar għall-ħxejjex (20,77 %)
English: Countries concerned: EU Member States and EFTA countries
Translation (en-mt): L-Istati Membri tal-UE u l-pajjiżi tal-EFTA
English: Under category 'Other' (foods supplements and soup and sauces) the percentage was 17%.
Translation (en-mt): Taħt il-kategorija "Oħrajn" (supplimenti tal-ikel u soppa u zlazi) il-perċentwal kien ta' 17 %.
English: Irradiation is used for sanitary and phytosanitary purposes to kill bacteria (such as Salmonella, Campylobacter and E. coli) that can cause food poisoning and to eliminate organisms harmful to plant or plant products such as insects and other pests.
Translation (en-mt): L-irradjazzjoni tintuża għal skopijiet fitosanitarji biex toqtol il-batterji (bħal Salmonella, Campylobacter u E. coli) li jistgħu jikkawżaw l-avvelenament mill-ikel u biex telimina organiżmi li huma ta' ħsara għall-pjanti jew prodotti tal-pjanti bħal insetti u pesti oħra.
English: At marketing stage, as illustrated in Figure 4, the majority of the products analysed were 'herbs and spices' (42%) and the 'cereals, seed, vegetables, fruit and their products' (22%).
Translation (en-mt): Fl-istadju tal-kummerċjalizzazzjoni, kif muri fil-Figura 4, il-maġġoranza tal-prodotti analizzati kienu "ħxejjex aromatiċi u ħwawar" (42 %) u "ċereali, żrieragħ, ħxejjex, frott u l-prodotti tagħhom" (22 %).
English: The treatment took place mainly in two Member States: Belgium, which treated two thirds of the irradiated food of the EU (68%), and the Netherlands (13%).
Translation (en-mt): Il-Belġju, li tratta żewġ terzi tal-ikel irradjat tal-UE (68 %), u n-Netherlands (13%).
English: Results of checks carried out in irradiation facilities in 2016-2017
Translation (en-mt): Ir-riżultati tal-kontrolli mwettqa fil-faċilitajiet tal-irradjazzjoni fl-2016-2017
English: Of those 14 Member States equipped with irradiation facilities, Bulgaria, Italy, Romania and the United Kingdom did not irradiate any foodstuffs over the period covered by this report.
Translation (en-mt): Minn dawk l-14-il Stat Membru mgħammra b'faċilitajiet tal-irradjazzjoni, il-Bulgarija, l-Italja, ir-Rumanija u r-Renju Unit ma rradjaw l-ebda oġġett ta' ikel fil-perjodu kopert minn dan ir-rapport.
English: Directive 1999/3/EC (implementing Directive) of the European Parliament and of the Council of 22 February 1999 on the establishment of a Community list of foods and food ingredients treated with ionising treatment.
Translation (en-mt): Id-Direttiva 1999/3/KE (Direttiva ta' Implimentazzjoni) tal-Parlament Ewropew u tal-Kunsill tat-22 ta' Frar 1999 dwar l-istabbiliment ta' lista Komunitarja ta' ikel u ta' ingredjenti tal-ikel ittrattati bir-radjazzjoni jonizzanti.
English: Malta did not submit any data for the year 2017.
Translation (en-mt): Malta ma ssottomettiet l-ebda data għas-sena 2017.
English: The two main commodities irradiated in the EU are frog legs (ca 57%) and dried aromatic herbs, spices and vegetables seasoning (ca 21%).
Translation (en-mt): Iż-żewġ prodotti ewlenin ittrattati bir-radjazzjoni fl-UE huma riġlejn iż-żrinġijiet (ca 57 %) u l-ħxejjex aromatiċi mnixxfin, il-ħwawar u l-ħwawar għall-ħxejjex (ca 21 %).
English: [7: GSK set up ViiV Healthcare as a joint venture with Pfizer in November 2009.
Translation (en-mt): [7: GSK stabbilit ViiV Healthcare bħala impriża konġunta ma' Pfizer f'Novembru 2009.
English: [6: COM(2015)0497 of 14 October 2015.]
Translation (en-mt): COM(2015)0497 tal-14 ta' Ottubru 2015.]
English: GlaxoSmithKline also registered Retrovir 300 mg x 60, Retrovir 250 mg x 40 and Trizivir 750 mg x 60 under the Regulation in 2004, but there were no sales under tiered prices of these products in the reporting period.
Translation (en-mt): GlaxoSmithKline rreġistrat ukoll Retrovir 300 mg x 60, Retrovir 250 mg x 40, u Trizivir 750 mg x 60 skont ir-Regolament fl-2004, iżda ma kienx hemm bejgħ taħt il-prezzijiet f'saffi ta' dawn il-prodotti matul il-perjodu ta' rapportar.
English: EVALUATION OF LIST OF COUNTRIES OF DESTINATION
Translation (en-mt): L-EVALWAZZJONI TA' LISTA TA' PAJJIŻI TA' DESTINAZZJONI
English: [1: OJ L 135, 24.5.2016, p. 39 (replacing Council Regulation (EC) No 953/2003)]
Translation (en-mt): [1: ĠU L 135, 24.5.2016, p. 39 (li jissostitwixxi r-Regolament tal-Kunsill (KE) Nru 953/2003)]
English: EPIVIR Oral Solution 10mg/ml 240 ml
Translation (en-mt): Soluzzjoni Orali EPIVIR 10mg/ml 240 ml
English: Countries of destination during the reporting period were: China, Honduras, Indonesia, Kenya, Moldova, Nigeria, South Africa, and Uganda.
Translation (en-mt): Il-pajjiżi ta' destinazzjoni matul il-perjodu tar-rappurtar kienu: iċ-Ċina, il-Ħonduras, l-Indoneżja, il-Kenja, il-Moldova, in-Niġerja, l-Afrika t'Isfel u l-Uganda.
English: One company, GlaxoSmithKline / ViiV Healthcare, has medicines registered under the Regulation.
Translation (en-mt): Kumpanija waħda, GlaxoSmithKline / ViiV Healthcare, għandha mediċini reġistrati skont dan ir-Regolament.
English: NOTIFICATIONS UNDER ARTICLE 10
Translation (en-mt): NOTIFIKI SKONT L-ARTICLE 10
English: Regulation (EU) 2016/793 to avoid trade diversion into the European Union of certain key medicines ("the Regulation"), adopted in May 2016, puts in place safeguards to prevent diversion of medicines from poor developing countries into the European Union.
Translation (en-mt): Ir-Regolament (UE) Nru 2016/793 sabiex tiġi evitata diversifikazzjoni fil-kummerċ fl-Unjoni Ewropea ta' ċerti mediċini prinċipali ("ir-Regolament"), adottat f'Mejju 2016, jistabbilixxi salvagwardji biex tkun evitata d-diversifikazzjoni ta' mediċini minn pajjiżi fqar li qed jiżviluppaw lejn l-Unjoni Ewropea.
English: REFIT EVALUATION OF THE REGULATION
Translation (en-mt): L-EVALWAZZJONI REFIT
English: The Regulation allows for the registration of medicines treating HIV/AIDS, malaria and tuberculosis.
Translation (en-mt): Ir-Regolament jippermetti r-reġistrazzjoni ta' mediċini li jittrattaw l-HIV/AIDS, il-malarja u t-tuberkolożi.
English: The EU contributes for example to the Global Fund to fight AIDS, tuberculosis and malaria that spends USD 3.5 billion a year in developing countries to which the EU collectively contributes about 50% and the Commission contributed EUR 370 million from the Development Cooperation Instrument and the European Development Fund for 2014-2016.
Translation (en-mt): L-UE tikkontribwixxi pereżempju għall-Fond Globali għall-ġlieda kontra l-AIDS, it-tuberkulożi u l-malarja li jonfoq USD 3.5 biljun fis-sena f'pajjiżi li qegħdin jiżviluppaw li għalih l-UE b'mod kollettiv tikkontribwixxi madwar 50% u l-Kummissjoni kkontribwiet EUR 370 miljun mill-Istrument ta' Koperazzjoni għall-Iżvilupp u mill-Fond Ewropew għall-Iżvilupp għall-2014-2016.
English: The evaluation concluded that the objective of improving access to medicines in the poorest developing countries remains relevant, that tiered pricing still has value, and that in view of the small administrative burden, the benefits that have been realised, the added value of a signal of support for tiered pricing, and its place in the overall context of action targeting major diseases, the Regulation still has a role in the future in the context of the Commission's aim, as stated in the Trade for all Communication, to promote an ambitious global health agenda and better access to medicines in poor countries.
Translation (en-mt): L-evalwazzjoni kkonkludiet li l-objettiv ta' titjib tal-aċċess għall-mediċini fl-ifqar pajjiżi li qed jiżviluppaw għadu rilevanti, li l-ipprezzar f'saffi għadu jiswa, u li minħabba l-piż amministrattiv żgħir, il-benefiċċji li nkisbu, il-valur miżjud ta' sinjal ta' appoġġ għall-ipprezzar f'saffi, u postu fil-kuntest ġenerali ta' azzjoni kontra mard maġġuri, ir-Regolament għad għandu rwol fil-futur fil-kuntest tal-għan tal-Kummissjoni, kif indikat fil-Komunikazzjoni Kummerċ għall-kulħadd, għall-promozzjoni ta' aġenda globali ambizzjuża għas-saħħa u aċċess aħjar għall-mediċini fil-pajjiżi l-fqar.
English: Report on the application of Regulation (EU) 2016/793 of the European Parliament and of the Council of 11 May 2016 to avoid trade diversion into the European Union of certain key medicines
Translation (en-mt): Rapport dwar l-implimentazzjoni tar-Regolament (UE) 2016/793 tal-Parlament Ewropew u tal-Kunsill tal-11 ta' Mejju 2016 sabiex tiġi evitata diversifikazzjoni fil-kummerċ fl-Unjoni Ewropea ta' ċerti mediċini prinċipali
English: GENERAL CRITERIA FOR THE IMPLEMENTATION OF ARTICLE 3
Translation (en-mt): KRITERJI ĠENERALI
English: ANNEX
Translation (en-mt): ANNESS
English: Ziagen 300mg x 60 Kenya 1,159 16.12
Translation (en-mt): Ziagen 300mg x 60 il-Kenja 1,159 16.
English: Product Country destinations Volume Avg. selling price ($)*
Translation (en-mt): Prodott Pajjiż ta' destinazzjoni Volum Prezz tal-bejgħ medju ($)*
English: ViiV Healthcare/GSK packs sold in 2015 under Regulation (EU) 2016/793 (in-country sales data)
Translation (en-mt): ViiV Healthcare/GSK pakketti mibjugħa fl-2015 skont ir-Regolament (UE) Nru 2016/793 (dejta dwar il-bejgħ fil-pajjiż)
English: Retrovir Oral Solution 10mg/ml 200ml Kenya 207 13.64
Translation (en-mt): Retrovir Oral Solution 10mg/ml 200ml il-Kenja 207 13.64
English: ViiV Healthcare/GSK packs sold in 2014 under Regulation (EU) 2016/793 (in-country sales data)
Translation (en-mt): ViiV Healthcare/GSK pakketti mibjugħa fl-2014 skont ir-Regolament (UE) Nru 2016/793 (dejta dwar il-bejgħ fil-pajjiż)
English: *includes distribution costs
Translation (en-mt): * jinkludi l-ispejjeż tad-distribuzzjoni
English: Epivir Oral Solution 10mg/ml 240 ml Honduras, Kenya, Moldova 541 21.69
Translation (en-mt): Epivir Oral Solution 10mg/ml 240 ml Il-Ħonduras, il-Kenja, il-Moldova 541 21.69
English: Retrovir Oral Solution 10mg/ml 200ml China, Kenya, Moldova 17,609 14.75
Translation (en-mt): Retrovir Oral Solution 10mg/ml 200ml Iċ-Ċina, il-Kenja, il-Moldova 17,609 14.75
English: (documents COM(2017)281 final - 2017/0123 (COD), COM(2017)278 final - 2017/0121 (COD) and COM(2017)277 final - 2017/0122 (COD) 01/06/2017
Translation (en-mt): (id-dokumenti COM(2017)281 final - 2017/0123 (COD), COM(2017)278 final - 2017/0121 (COD) u COM(2017)277 final - 2017/0122 (COD) 01/06/2017
English: Regular return of the driver
Translation (en-mt): Ritorn regolari tax-xufier
English: Introduction of new tachograph technology
Translation (en-mt): L-introduzzjoni ta' teknoloġija tat-takografu ġdida
English: Date of the opinion of the Committee of the Regions: 01/02/2018
Translation (en-mt): Data tal-opinjoni tal-Kumitat tar-Reġjuni: 01/02/2018
English: position of the Council on the adoption of a Regulation amending Regulation (EC) No 1071/2009, Regulation (EC) No 1072/2009 and Regulation (EU) No 1024/2012 with a view to adapting them to developments in the sector, a Regulation amending Regulation (EC) No 561/2006 on minimum requirements on maximum daily and weekly driving times, minimum breaks and daily and weekly rest periods and Regulation (EU) 165/2014 as regards positioning by means of tachographs and a Directive amending Directive 2006/22/EC as regards enforcement requirements and laying down specific rules with respect to Directive 96/71/EC and Directive 2014/67/EU for posting drivers in the road transport sector and amending Regulation (EU) No 1024/2012
Translation (en-mt): il-pożizzjoni tal-Kunsill dwar l-adozzjoni ta' Regolament li jemenda r-Regolament (KE) Nru 1071/2009, ir-Regolament (KE) Nru 1072/2009 u r-Regolament (UE) Nru 1024/2012 bl-għan li jiġu adattati għall-iżviluppi fis-settur, ta' Regolament li jemenda r-Regolament (KE) Nru 561/2006 fir-rigward tar-rekwiżiti minimi dwar il-ħinijiet massimi tas-sewqan ta' kuljum u fil-ġimgħa, id-durata minima tal-pawżi u tal-perjodi ta' mistrieħ ta' kuljum u fil-ġimgħa u r-Regolament (UE) Nru 165/2014 fir-rigward tal-lokalizzazzjoni permezz ta' takografi u ta' Direttiva li temenda d-Direttiva 2006/22/KE fir-rigward ta' rekwiżiti tal-infurzar u li tistabbilixxi regoli speċifiċi fir-rigward tad-Direttiva 96/71/KE u d-Direttiva 2014/67/UE għall-istazzjonar tax-xufiera fis-settur tat-trasport bit-triq u li temenda r-Regolament (UE) Nru 1024/2012
English: Date of adoption of the position of the Council: 07/04/2020
Translation (en-mt): Data tal-adozzjoni tal-pożizzjoni tal-Kunsill: 07/04/2020
English: Establishment criteria relating to drivers (Rome I)
Translation (en-mt): Kriterji ta' stabbiliment relatati max-xufiera (Ruma I)
English: The Council position specifies a time schedule for the uptake of this new technology in new vehicles (two years from the date of adoption of the technical specifications) and in the existing fleet (retrofit three years from the date of adoption of the technical specifications for all vehicles equipped with a tachograph other than the smart tachograph version 1; retrofit four years from the date of adoption of the technical specifications for all vehicles equipped with a smart tachograph version 1).
Translation (en-mt): Il-pożizzjoni tal-Kunsill tispeċifika skeda ta' żmien għall-użu ta' din it-teknoloġija ġdida f'vetturi ġodda (sentejn mid-data tal-adozzjoni tal-ispeċifikazzjonijiet tekniċi) u fil-flotta eżistenti (modifika retroattiva tliet snin mid-data tal-adozzjoni tal-ispeċifikazzjonijiet tekniċi għall-vetturi kollha mgħammra b'takografu għajr il-verżjoni 1 tat-takografu intelliġenti; modifika retroattiva erba' snin mid-data tal-adozzjoni tal-ispeċifikazzjonijiet tekniċi għall-vetturi kollha mgħammra bil-verżjoni 1 tat-takografu intelliġenti).
English: pursuant to Article 294(6) of the Treaty on the Functioning of the European Union
Translation (en-mt): skont l-Artikolu 294(6) tat-Trattat dwar il-Funzjonament tal-Unjoni Ewropea
English: Date of the opinion of the European Economic and Social Committee: 18/01/2018
Translation (en-mt): Data tal-opinjoni tal-Kumitat Ekonomiku u Soċjali Ewropew: 18/01/2018
English: The Commission can accept the idea of a cooling-off period, to deal with the issue of "systematic cabotage", i.e. operators repeating several consecutive periods of cabotage in the same Member State, by leaving and re-entering that Member State, in violation of the limits imposed by Regulation (EU) No 1072/2009, maintained in the amending text.
Translation (en-mt): Il-Kummissjoni tista' taċċetta l-idea ta' perjodu ta' preklużjoni biex tindirizza l-kwistjoni ta' "kabotaġġ sistematiku", jiġifieri fejn l-operaturi jirrepetu diversi perjodi konsekuttivi ta' kabotaġġ fl-istess Stat Membru, billi joħorġu minn dak l-Istat Membru u jerġgħu jidħlu fih, li jikkostitwixxi ksur tal-limiti imposti mir-Regolament (UE) Nru 1072/2009, miżmuma fit-test ta' emenda.
English: The revised enforcement directive (Directive 2006/22/EC) and the lex specialis on the posting of workers will have a date of transposition of the national measures by the Member States of 18 months from the entry into force of the act.
Translation (en-mt): Id-Direttiva riveduta dwar l-infurzar (id-Direttiva 2006/22/KE) u l-lex specialis dwar l-istazzjonar tal-ħaddiema se jkollhom data ta' traspożizzjoni tal-miżuri nazzjonali mill-Istati Membri ta' 18-il xahar mid-dħul fis-seħħ tal-att.
English: Rules on cabotage
Translation (en-mt): Regoli dwar il-kabotaġġ
English: (2) A proposal to amend Regulation 561/2006 on driving and rest time rules in road transport and Regulation 165/2014 on the tachograph;
Translation (en-mt): (2) Proposta biex jiġi emendat ir-Regolament 561/2006 fir-rigward tar-regoli dwar il-ħin tas-sewqan u ta' mistrieħ fit-trasport bit-triq u r-Regolament 165/2014 fir-rigward tat-takografu;
English: Whereas the revised Regulations (EC) No 561/2006 and 165/2014 will be applicable immediately upon entry into force, they include transitional provisions for the application of the provisions related to the implementation of the smart tachograph (see above) and the application of the rules to light commercial vehicles (from 1 July 2026).
Translation (en-mt): Billi r-Regolamenti riveduti (KE) Nru 561/2006 u 165/2014 se jkunu applikabbli mill-ħin li jiddaħħlu fis-seħħ, dawn jinkludu dispożizzjonijiet tranżitorji għall-applikazzjoni tad-dispożizzjonijiet relatati mal-implimentazzjoni tat-takografu intelliġenti (ara hawn fuq) u mal-applikazzjoni tar-regoli għal vetturi kummerċjali ħfief (mill-1 ta' Lulju 2026).
English: Date of the position of the European Parliament, first reading: 04/04/2019
Translation (en-mt): Data tal-pożizzjoni tal-Parlament Ewropew, fl-ewwel qari: 04/04/2019
English: (3) A proposal to amend Directive 2006/22/EC on minimum requirements for controlling compliance with the driving and resting time rules and to establish sector specific rules for posting of drivers (lex specialis to posted workers Directive 96/71/EC and to its enforcement Directive 2014/67/EU).
Translation (en-mt): (3) Proposta biex tiġi emendata d-Direttiva 2006/22/KE fir-rigward tal-kundizzjonijiet minimi għall-kontroll tal-konformità mar-regoli tal-ħin tas-sewqan u tal-mistrieħ u biex jiġu stabbiliti regoli speċifiċi għas-settur għall-istazzjonar tax-xufiera (lex specialis għad-Direttiva 96/71/KE rigward ix-xufiera stazzjonati u għad-Direttiva 2014/67/UE dwar l-infurzar tagħha).
English: EN EN
Translation (en-mt): A.
English: What is the problem being addressed?
Translation (en-mt): X'inhi l-problema li qed tiġi indirizzata?
English: Executive Summary Sheet
Translation (en-mt): Skeda tas-Sommarju Eżekuttiv
English: Why?
Translation (en-mt): C.
English: C. Impacts of the preferred option
Translation (en-mt): Impatti tal-għażla ppreferuta