COMMISSION IMPLEMENTING REGULATION (EU) 2017/555 of 24 March 2017 amending Implementing Regulation (EU) No 540/2011 as regards the extension of the

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1 COMMISSION IMPLEMENTING REGULATION (EU) 2017/555 of 24 March 2017 amending Implementing Regulation (EU) No 540/2011 as regards the extension of the approval periods of several active substances listed in Part B of the Annex to Implementing Regulation (EU) No 686/2012 (AIR IV renewal programme) 1

2 KOMMISJONENS GJENNOMFØRINGSFORORDNING (EU) 2017/555 av 24. mars 2017 om endring av gjennomføringsforordning (EU) nr. 540/2011 med hensyn til forlengelse av godkjenningsperioden for flere aktive stoffer oppført i del B i vedlegget til gjennomføringsforordning (EU) nr. 686/2012 (fornyelsesprogram AIR IV) EUROPAKOMMISJONEN HAR under henvisning til traktaten om Den europeiske unions virkemåte, under henvisning til europaparlaments- og rådsforordning (EF) nr. 1107/2009 av 21. oktober 2009 om omsetning av plantevernmidler og om oppheving av rådsdirektiv 79/117/EØF og 91/414/EØF( 1 ), særlig artikkel 17 første ledd og artikkel 78 nr. 2, og ut fra følgende betraktninger: 1) I del A i vedlegget til Kommisjonens gjennomføringsforordning (EU) nr. 540/2011( 2 ) angis de aktive stoffene som anses som godkjent i henhold til forordning (EF) nr. 1107/ ) I samsvar med Kommisjonens gjennomføringsforordning (EU) nr. 844/2012( 3 ) er det inngitt søknader om fornyelse av godkjenning av de aktive stoffene i denne forordning. Godkjenningen av disse stoffene kan imidlertid utløpe av årsaker som er utenfor søkerens kontroll, før det er truffet beslutning om fornyelse av godkjenningen. Godkjenningsperiodene bør derfor forlenges i samsvar med artikkel 17 i forordning (EF) nr. 1107/ ) Med hensyn til tiden og ressursene som kreves for å vurdere søknader om fornyelse av godkjenninger for det store antallet aktive stoffer som utløper mellom 2019 og 2021, ble det ved Kommisjonens gjennomføringsbeslutning K(2016)6104( 4 ) opprettet et arbeidsprogram som grupperte aktive stoffer som ligner på hverandre, og fastsatte prioriteringer på grunnlag av sikkerhetsrisiko for menneskers og dyrs helse eller miljøet, som fastsatt i artikkel 18 i forordning (EF) nr. 1107/ ) Stoffer som antas å være lavrisikostoffer, bør prioriteres i samsvar med gjennomføringsbeslutning K(2016)6104. Godkjenningen av disse stoffene bør derfor forlenges med en så kort periode som mulig. Idet det tas hensyn til fordelingen av ansvar og arbeid mellom medlemsstatene som opptrer som rapportører og medrapportører og tilgjengelige ressurser som er nødvendige for vurdering og beslutningstaking, bør nevnte periode være ett år for de aktive stoffene parafinolje (CAS-nr ), parafinolje (CAS-nr ), parafinolje (CAS-nr ), parafinolje (CAS-nr ) og svovel. ( 1 ) EUT L 309 av , s. 1. ( 2 ) EUT L 153 av , s. 1. ( 3 ) Kommisjonens gjennomføringsforordning (EU) nr. 844/2012 av 18. september 2012 om fastsettelse av de bestemmelsene som er nødvendige for gjennomføring av framgangsmåten for fornyelse for aktive stoffer som fastsatt i europaparlaments- og rådsforordning (EF) nr. 1107/2009 om omsetning av plantevernmidler (EUT L 252 av , s. 26). ( 4 ) Kommisjonens gjennomføringsbeslutning av 28. september 2016 om opprettelse av et arbeidsprogram for vurdering av søknader om fornyelse av godkjenninger av aktive stoffer som utløper i 2019, 2020 og 2021, i samsvar med europaparlaments- og rådsforordning (EF) nr. 1107/2009 (EUT C 357 av , s. 9).

3 3 5) For aktive stoffer som ikke tilhører de prioriterte kategoriene i gjennomføringsbeslutning K(2016)6104, bør godkjenningsperioden forlenges med to eller tre år, idet det tas hensyn til nåværende utløpsdato, det faktum at den utfyllende dokumentasjonen for et aktivt stoff i henhold til artikkel 6 nr. 3 i gjennomføringsforordning (EU) nr. 844/2012 skal legges fram senest 30 måneder før godkjenningen utløper, behovet for å sørge for en jevn arbeids- og ansvarsfordeling mellom medlemsstatene som er rapportører og medrapportører, og ressursene som kreves til vurdering og beslutningstaking. Det er derfor hensiktsmessig å forlenge godkjenningsperioden for 2-fenylfenol (herunder saltene, for eksempel natriumsalt), klormekvat, dimetaklor, etofenproks, penkonazol, propakvizafop, tetrakonazol, triallat og zeta-cypermetrin med to år, og å utvide godkjenningsperioden for de aktive stoffene bensulfuron, natrium-5-nitroguaiakolat, natrium-onitrofenolat, natrium-p-nitrofenolat og tebufenpyrad med 3 år. 6) Kommisjonen har mottatt en søknad om fornyelse av godkjenningen av det aktive stoffet kizalofop-p (varianten kizalofop-p-etyl) og en egen søknad om fornyelse av godkjenningen av det aktive stoffet kizalofop-p (varianten kizalofop-ptefuryl). I betraktning av dette og på grunn av ulike risikoprofilene for kizalofop-p-etyl og kizalofop-p-tefuryl, er det hensiktsmessig å anse dem som to ulike aktive stoffer i forbindelse med framgangsmåten for fornyelse. Varianten kizalofop-p-etyl tilhører ikke de prioriterte kategoriene i gjennomføringsbeslutning K(2016)6104. Av denne grunn, og idet det tas hensyn til begrunnelsene gitt i betraktning 5, er det hensiktsmessig å forlenge godkjenningsperioden med to år. 7) Med tanke på formålet med artikkel 17 første ledd i forordning (EF) nr. 1107/2009 vil Kommisjonen i tilfeller der det ikke er framlagt utfyllende dokumentasjon i samsvar med gjennomføringsforordning (EU) nr. 844/2012 senest 30 måneder før den respektive utløpsdatoen fastsatt i vedlegget til denne forordning, fastsette utløpsdatoen til samme dato som gjaldt før denne forordning, eller tidligst mulige dato deretter. 8) Med tanke på formålet med artikkel 17 første ledd i forordning (EF) nr. 1107/2009 vil Kommisjonen i tilfeller der den vedtar en forordning om at godkjenningen av et aktivt stoff nevnt i vedlegget til denne forordning ikke fornyes fordi godkjenningskriteriene ikke er oppfylt, fastsette utløpsdatoen til samme dato som gjaldt før ikrafttredelsen av denne forordning, eller til ikrafttredelsesdatoen for forordningen om at godkjenningen av det aktive stoffet ikke fornyes, avhengig av hvilken dato som faller sist. Dersom Kommisjonen vedtar en forordning om fornyelse av godkjenningen av et aktivt stoff nevnt i vedlegget til denne forordning skal den, avhengig av omstendighetene, bestrebe seg på å fastsette den tidligst mulige anvendelsesdatoen. 9) Gjennomføringsforordning (EU) nr. 540/2011 bør derfor endres. 10) Idet det tas hensyn til at godkjenningen av noen av stoffene utløper 31. oktober 2019, og at søkere bør legge fram utfyllende dokumentasjon 30 måneder før godkjenningen utløper, bør denne forordning tre i kraft så snart som mulig. 11) Tiltakene fastsatt i denne forordning er i samsvar med uttalelse fra Den faste komité for planter, dyr, næringsmidler og fôr VEDTATT DENNE FORORDNING: Artikkel 1 Vedlegget til gjennomføringsforordning (EU) nr. 540/2011 endres i samsvar med vedlegget til denne forordning. Artikkel 2 Denne forordning trer i kraft den tredje dagen etter at den er kunngjort i Den europeiske unions tidende.

4 Denne forordning er bindende i alle deler og kommer direkte til anvendelse i alle medlemsstater. Utferdiget i Brussel 24. mars For Kommisjonen Jean-Claude JUNCKER President

5 5 VEDLEGG I del A i vedlegget til gjennomføringsforordning (EU) nr. 540/2011 gjøres følgende endringer: 1) I rad 271 om bensulfuron endres datoen i sjette kolonne, «Godkjenningen utløper», til «31. oktober 2022». 2) I rad 272 om natrium-5-nitroguaiakolat endres datoen i sjette kolonne, «Godkjenningen utløper», til «31. oktober 2022». 3) I rad 273 om natrium-o-nitrofenolat endres datoen i sjette kolonne, «Godkjenningen utløper», til «31. oktober 2022». 4) I rad 274 om natrium-p-nitrofenolat endres datoen i sjette kolonne, «Godkjenningen utløper», til «31. oktober 2022». 5) I rad 275 om tebufenpyrad endres datoen i sjette kolonne, «Godkjenningen utløper», til «31. oktober 2022». 6) I rad 276 om klormekvat endres datoen i sjette kolonne, «Godkjenningen utløper», til «30. november 2021». 7) I rad 278 om propakvizafop endres datoen i sjette kolonne, «Godkjenningen utløper», til «30. november 2021». 8) I rad 281 om zeta-cypermetrin endres datoen i sjette kolonne, «Godkjenningen utløper», til «30. november 2021». 9) I rad 284 om dimetaklor endres datoen i sjette kolonne, «Godkjenningen utløper», til «31. desember 2021». 10) I rad 285 om etofenproks endres datoen i sjette kolonne, «Godkjenningen utløper», til «31. desember 2021». 11) I rad 287 om penkonazol endres datoen i sjette kolonne, «Godkjenningen utløper», til «31. desember 2021». 12) I rad 288 om triallat endres datoen i sjette kolonne, «Godkjenningen utløper», til «31. desember 2021». 13) I rad 292 om svovel endres datoen i sjette kolonne, «Godkjenningen utløper», til «31. desember 2020». 14) I rad 293 om tetrakonazol endres datoen i sjette kolonne, «Godkjenningen utløper», til «31. desember 2021». 15) I rad 294 om parafinoljer endres datoen i sjette kolonne, «Godkjenningen utløper», til «31. desember 2020». 16) I rad 295 om parafinolje endres datoen i sjette kolonne, «Godkjenningen utløper», til «31. desember 2020». 17) I rad 299 om 2-fenylfenol (herunder saltene, for eksempel natriumsalt) endres datoen i sjette kolonne, «Godkjenningen utløper», til «31. desember 2021».

6 18) Posten med referansenummer 279 skal lyde: «279 Kizalofop-P Kizalofop-Ptefuryl tetrahydrofur- (RS)- CAS-nr furyl-(r)-2-[ (6- CIPAC-nr. klorkinoksalin yloksy)fenoksy]propi onat Kizalofop-P-etyl etyl (R)-2-[4-(6- CAS-nr klorkinoksalin CIPAC-nr. yloksy)fenoksy]propi onat 795 g/kg 950 g/kg 1. desember desember november november 2021 DEL A Bare bruk som ugressmiddel kan tillates. DEL B Ved gjennomføringen av de ensartede prinsippene nevnt i artikkel 29 nr. 6 i forordning (EF) nr. 1107/2009, skal det tas hensyn til konklusjonene i den sammenfattende rapporten om kizalofop-p, særlig tillegg I og II til denne, som sluttbehandlet av Den faste komité for næringsmiddelkjeden og dyrehelsen 23. januar Ved denne samlede vurderingen skal medlemsstatene rette særlig oppmerksomhet mot følgende: spesifikasjonen til det tekniske materialet slik det produseres kommersielt, som skal bekreftes og dokumenteres ved hjelp av relevante analysedata. Analysestoffet som brukes i toksisitetsdokumentasjonen, bør sammenholdes med og kontrolleres mot spesifikasjonen til det tekniske materialet, sikkerheten for brukere og arbeidstakere, og sørge for at bruksvilkårene fastsetter bruk av hensiktsmessig personlig verneutstyr, vern av planter utenfor målgruppen og sørge for at godkjenningsvilkårene om nødvendig omfatter risikoreduserende tiltak, for eksempel buffersoner, Godkjenningsvilkårene skal om nødvendig omfatte risikoreduserende tiltak.

7 7 De berørte medlemsstatene skal sørge for at melderen framlegger for Kommisjonen ytterligere opplysninger om risikoen for leddyr utenfor målgruppen. De skal sørge for at melderen framlegger slike opplysninger for Kommisjonen innen 30. november 2011.»

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