Leit í EES-gagnagrunni
Commission Implementing Regulation (EU) 2023/937 of 10 May 2023 correcting Implementing Regulation (EU) 2017/2470 as regards the inclusion of ‘Phosphated distarch phosphate produced from wheat starch’ in the Union list of novel foods
Framkvæmdarreglugerð framkvæmdastjórnarinnar (ESB) 2023/937 frá 10. maí 2023 um leiðréttingu á framkvæmdarreglugerð (ESB) 2017/2470 að því er varðar færslu fosfataðs dísterkjufosfats sem er framleitt úr hveitisterkju á skrá Sambandsins yfir nýfæði
Commission Implementing Regulation (EU) 2023/932 of 8 May 2023 amending Implementing Regulation (EU) No 540/2011 as regards the approval period of the active substance pyridalyl
Framkvæmdarreglugerð framkvæmdastjórnarinnar (ESB) 2023/932 frá 8. maí 2023 um breytingu á framkvæmdarreglugerð (ESB) nr. 540/2011 að því er varðar samþykkistímabil fyrir virka efnið pýridalýl
Commission Implementing Regulation (EU) 2023/931 of 8 May 2023 amending Implementing Regulation (EU) 2017/2470 as regards the conditions of use of the traditional food from a third country infusion from coffee leaves of Coffea arabica L. and/or Coffea canephora Pierre ex A. Froehner
Framkvæmdarreglugerð framkvæmdastjórnarinnar (ESB) 2023/931 frá 8. maí 2023 um breytingu á framkvæmdarreglugerð (ESB) 2017/2470 að því er varðar skilyrði fyrir notkun hefðbundinna matvæla frá þriðja landi sem eru seyði úr kaffilaufum af Coffea arabica L. og/eða Coffea canephora Pierre ex A. Froehner
Commission Regulation (EU) 2023/915 of 25 April 2023 on maximum levels for certain contaminants in food and repealing Regulation (EC) No 1881/2006
Commission Implementing Decision (EU) 2023/910 of 3 May 2023 amending Implementing Decision (EU) 2019/450 as regards the publication of references of European Assessment Documents for corrugated bitumen tiles or sheets and other construction products
Proposal for a Regulation of the European Parliament and of the Council on the supplementary protection certificate for medicinal products (recast)
Proposal for a Regulation of the European Parliament and of the Council on the supplementary protection certificate for plant protection products (recast)
Proposal for a Regulation of the European Parliament and of the Council on the unitary supplementary certificate for medicinal products, and amending Regulation (EU) 2017/1001, Regulation (EC) No 1901/2006 as well as Regulation (EU) No 608/2013
Proposal for a Regulation of the European Parliament and of the Council on the unitary supplementary protection certificate for plant protection products
Proposal for a Directive of the European Parliament and of the Council on the Union code relating to medicinal products for human use, and repealing Directive 2001/83/EC and Directive 2009/35/EC
C(2023)2672
Commission Delegated Regulation (EU) 2023/1434 of 25 April 2023 amending, for the purposes of its adaptation to technical and scientific progress, Regulation (EC) No 1272/2008 of the European Parliament and of the Council on classification, labelling and packaging of substances and mixtures as regards the addition of notes to Part 1, section 1.1.3, of Annex VI
Framseld reglugerð framkvæmdastjórnarinnar (ESB) 2023/1434 frá 25. apríl 2023 um breytingu á reglugerð Evrópuþingsins og ráðsins (EB) nr. 1272/2008 um flokkun, merkingu og pökkun efna og blandna, að því er varðar að bæta athugasemdum við lið 1.1.3 í 1. hluta VI. viðauka, í því skyni að laga hana að tæknilegum og vísindalegum framförum
Proposal for a Directive of the European Parliament and of the Council amending Council Directives 2001/110/EC relating to honey, 2001/112/EC relating to fruit juices and certain similar products intended for human consumption, 2001/113/EC relating to fruit jams, jellies and marmalades and sweetened chestnut purée intended for human consumption, and 2001/114/EC relating to certain partly or wholly dehydrated preserved milk for human consumption
Proposal for a Regulation of the European Parliament and of the Council laying down Union procedures for the authorisation and supervision of medicinal products for human use and establishing rules governing the European Medicines Agency, amending Regulation (EC) No 1394/2007 and Regulation (EU) No 536/2014 and repealing Regulation (EC) No 726/2004, Regulation (EC) No 141/2000 and Regulation (EC) No 1901/2006
Commission Implementing Regulation (EU) 2023/859 of 25 April 2023 amending Implementing Regulation (EU) 2017/2470 as regards the specifications of the novel food 2’-Fucosyllactose (microbial source) to authorise its production by a derivative strain of Corynebacterium glutamicum ATCC 13032
Framkvæmdarreglugerð framkvæmdastjórnarinnar (ESB) 2023/859 frá 25. apríl 2023 um breytingu á framkvæmdarreglugerð (ESB) 2017/2470 að því er varðar nákvæmar skilgreiningar á nýfæðinu 2’-fúkósýllaktósa (örverufræðilegur uppruni) til að leyfa framleiðslu þess með notkun á afleiddum stofni Corynebacterium glutamicum ATCC 13032
Commission Regulation (EU) 2023/826 of 17 April 2023 laying down ecodesign requirements for off mode, standby mode, and networked standby energy consumption of electrical and electronic household and office equipment pursuant to Directive 2009/125/EC of the European Parliament and of the Council and repealing Commission Regulations (EC) No 1275/2008 and (EC) No 107/2009
Commission Implementing Regulation (EU) 2023/754 of 12 April 2023 granting a Union authorisation for the single biocidal product ‘Arche Chlorine’ in accordance with Regulation (EU) No 528/2012 of the European Parliament and of the Council
Commission Implementing Regulation (EU) 2023/753 of 12 April 2023 granting a Union authorisation for the biocidal product family “C(M)IT/MIT formulations”
Commission Implementing Decision (EU) 2023/733 of 3 April 2023 designating Union testing facilities for radio equipment and toys in accordance with Regulation (EU) 2019/1020 of the European Parliament and of the Council
Commission Implementing Decision .../... on the authorisation to place on the Union market in accordance with Regulation (EU) 2017/745 of the European Parliament and of the Council certain medical devices manufactured by Maquet Cardiopulmonary GmbH
Commission Regulation (EU) 2023/710 of 30 March 2023 amending Annexes II, III and V to Regulation (EC) No 396/2005 of the European Parliament and of the Council as regards maximum residue levels for bromopropylate, chloridazon, fenpropimorph, imazaquin and tralkoxydim in or on certain products
Reglugerð framkvæmdastjórnarinnar (ESB) 2023/710 frá 30. mars 2023 um breytingu á II., III. og V. viðauka við reglugerð Evrópuþingsins og ráðsins (EB) nr. 396/2005 að því er varðar hámarksgildi leifa fyrir brómóprópýlat, klórídasón, fenprópímorf, ímasakín og tralkoxýdím í eða á tilteknum afurðum
Commission Implementing Regulation (EU) 2023/708 of 20 March 2023 granting a Union authorisation for the biocidal product family ‘HYPO-CHLOR Product Family’ in accordance with Regulation (EU) No 528/2012 of the European Parliament and of the Council
Proposal for a Regulation of the European Parliament and of the Council on the approval and market surveillance of non-road mobile machinery circulating on public roads and amending Regulation (EU) 2019/1020
D087673/02
Commission Implementing Regulation (EU) 2023/741 of 5 April 2023 concerning the non-renewal of the approval of the active substance oxamyl, in accordance with Regulation (EC) No 1107/2009 of the European Parliament and of the Council, and amending Commission Implementing Regulation (EU) No 540/2011
Framkvæmdarreglugerð framkvæmdastjórnarinnar (ESB) 2023/741 frá 5. apríl 2023 um að endurnýja ekki samþykki fyrir virka efninu oxamýli, í samræmi við reglugerð Evrópuþingsins og ráðsins (EB) nr. 1107/2009, og um breytingu á framkvæmdarreglugerð framkvæmdastjórnarinnar (ESB) nr. 540/2011
D088558/01
Commission Implementing Regulation (EU) 2023/918 of 4 May 2023 amending Implementing Regulation (EU) No 540/2011 as regards the extension of the approval periods of the active substances aclonifen, ametoctradin, beflubutamid, benthiavalicarb, boscalid, captan, clethodim, cycloxydim, cyflumetofen, dazomet, diclofop, dimethomorph, ethephon, fenazaquin, fluopicolide, fluoxastrobin, flurochloridone, folpet, formetanate, Helicoverpa armigera nucleopolyhedrovirus, hymexazol, indolylbutyric acid, mandipropamid, metalaxyl, metaldehyde, metam, metazachlor, metribuzin, milbemectin, paclobutrazol, penoxsulam, phenmedipham, pirimiphos-methyl, propamocarb, proquinazid, prothioconazole, S-metolachlor, Spodoptera littoralis nucleopolyhedrovirus, Trichoderma asperellum strain T34 and Trichoderma atroviride strain I-1237
Framkvæmdarreglugerð framkvæmdastjórnarinnar (ESB) 2023/918 frá 4. maí 2023 um breytingu á framkvæmdarreglugerð (ESB) nr. 540/2011 að því er varðar framlengingu á samþykkistímabilum fyrir virku efnin aklónífen, ametóktradín, beflúbútamíð, benþíavalíkarb, boskalíð, kaptan, kletódím, sýkloxýdím, sýflúmetófen, dasómet, díklófóp, dímetómorf, etefón, fenasakín, flúópíkólíð, flúoxastróbín, flúrklóridón, fólpet, formetanat, Helicoverpa armigera-kjarnmargflötungaveiru, hýmexasól, indólýlsmjörsýru, mandíprópamíð, metalaxýl, metaldehýð, metam, metasaklór, metríbúsín, milbemektín, paklóbútrasól, penoxsúlam, fenmedífam, pírimífosmetýl, própamókarb, prókínasíð, próþíókónasól, S-metólaklór, Spodoptera littoralis-kjarnmargflötungaveiru, Trichoderma asperellum af stofni T34 og Trichoderma atroviride af stofni I-1237
D088783/01
Commission Regulation (EU) 2023/1490 of 19 July 2023 amending Regulation (EC) No 1223/2009 of the European Parliament and of the Council as regards the use in cosmetic products of certain substances classified as carcinogenic, mutagenic or toxic for reproduction
Reglugerð framkvæmdastjórnarinnar (ESB) 2023/1490 frá 19. júlí 2023 um breytingu á reglugerð Evrópuþingsins og ráðsins (EB) nr. 1223/2009 að því er varðar notkun á tilteknum efnum, sem eru flokkuð sem krabbameinsvaldandi, stökkbreytandi eða sem efni sem hafa eiturhrif á æxlun, í snyrtivörur