Information on biocides

Information on biocides

Information on biocides

Hawnhekk tista’ ssib informazzjoni dwar prodotti bijoċidali awtorizzati fis-suq tal-UE/taż-ŻEE, f’konformità mad-Direttiva dwar il-Prodotti Bijoċidali (Direttiva 98/8/KE) jew ir-Regolament dwar il-Prodotti Bijoċidali (Regolament (UE) Nru 528/2012).

Il-prodotti bijoċidali kollha li fihom sustanzi attivi approvati jiġu evalwati għas-sikurezza u l-effikaċja qabel ma jitħallew jinbiegħu fl-UE. Madankollu, il-prodotti li kienu fis-suq qabel l-2000 jistgħu jkomplu jinbiegħu filwaqt li l-awtoritajiet qed jevalwaw is-sustanzi attivi li fihom.

Kif għandek tfittex

Tista’ tfittex prodotti bijoċidali permezz ta’:

Isem kummerċjali tal-prodott;

Tip ta’ prodott;

Sustanza attiva fil-prodott (tinkludi l-għażla li tfittex permezz ta’ sustanzi attivi magħrufa bħala kandidati għas-sostituzzjoni);

Data dwar l-awtorizzazzjoni, (pereżempju detentur tal-awtorizzazzjoni jew numru tal-awtorizzazzjoni);

Dettalji dwar il-prodott, pereżempju informazzjoni dwar l-użu, bħall-organiżmu fil-mira u l-metodu ta’ applikazzjoni ta’ prodott, jew dikjarazzjonijiet ta’ periklu u ta’ prekawzjoni).

Tipi ta’ awtorizzazzjonijiet tal-prodott

Hija disponibbli informazzjoni minn tliet tipi ta’ awtorizzazzjoni:

Awtorizzazzjonijiet ssimplifikati: Dawn il-prodotti bijoċidali għandhom profil ambjentali jew tas-saħħa tal-bniedem u tal-annimali aktar favorevoli u għalhekk isegwu proċedura aktar sempliċi. L-awtorizzazzjoni tiġi ppubblikata flimkien man-notifiki relatati għat-tqegħid fis-suq ta’ prodott bijoċidali.

Awtorizzazzjonijiet tal-Unjoni: Dawn il-prodotti bijoċidali huma permessi li jitqiegħdu fis-suq fl-UE/fiż-ŻEE kollha u fl-Iżvizzera.

Awtorizzazzjonijiet nazzjonali: Dawn il-prodotti bijoċidali huma awtorizzati f’pajjiżi speċifiċi tal-UE. L-awtorizzazzjoni tiġi ppubblikata flimkien mar-rikonoxximenti reċiproċi relatati fl-Istati Membri l-oħra fejn il-prodott bijoċidali jkun ġie permess fis-suq.

Kif tiġi ppreżentata l-informazzjoni

Il-prodotti bijoċidali huma ppreżentati bħala gruppi ta’ awtorizzazzjonijiet, raggruppamenti ta’ prodotti, fejn ir-rikonoxximenti reċiproċi (estensjonijiet tal-awtorizzazzjoni nazzjonali tal-prodott għal żoni oħra tas-swieq) jiġu ppreżentati bl-awtorizzazzjonijiet ta’ referenza tagħhom. Dan jippermettilek tittraċċa l-oqsma kollha tas-suq fejn jitqiegħed prodott speċifiku kif ukoll l-ismijiet kummerċjali kollha li taħthom jitqiegħed prodott fis-suq. Il-prodotti awtorizzati permezz tal-istess proċedura ta’ awtorizzazzjoni tal-prodotti bijoċidali għandhom ir-raggruppamenti tagħhom stess.

Il-prinċipju tar-raggruppament tal-prodotti huwa applikat ukoll għat-tfittxijiet. Dan ifisser li t-tabella tar-riżultati turi raggruppamenti ta’ prodotti li fihom tal-inqas awtorizzazzjoni waħda li tissodisfa l-kriterji ta’ tiftix. Għalhekk, jekk tfittex pereżempju billi tfittex l-istatus tal-awtorizzazzjoni “awtorizzat”, se tirkupra r-raggruppamenti tal-prodotti kollha fejn mill-inqas awtorizzazzjoni waħda jkun fiha dan l-istatus speċifiku.

It-tabella tar-riżultati tippreżenta informazzjoni dwar il-livell tar-raggruppament tal-prodott, filwaqt li aktar informazzjoni dwar awtorizzazzjonijiet speċifiċi tal-prodott tista’ tinstab fl-iskeda informattiva dwar il-prodott. Kull prodott għandu skeda informattiva dedikata li żżomm informazzjoni dwar l-ismijiet kummerċjali applikabbli, id-dokumenti u d-detenturi tal-awtorizzazzjoni għal kull awtorizzazzjoni tal-prodott individwali, inkluża l-istorja tal-valutazzjoni tal-prodott. L-iskeda informattiva hija aċċessibbli permezz tal-ikona tal-għajn fit-tabella tar-riżultati.

Qabbel prodotti bijoċidali

Tista’ tqabbel sa erba’ prodotti biex tara l-karatteristiċi tagħhom, bħas-sustanzi attivi fil-prodott, il-konċentrazzjonijiet tagħhom, l-informazzjoni dwar l-użu tal-prodott u d-dikjarazzjonijiet ta’ periklu u ta’ prekawzjoni.

Il-biċċa l-kbira tal-informazzjoni fl-għodda ta’ tqabbil ġejja mis-sommarju tal-karatteristiċi tal-prodott (SPC). L-SPC huwa disponibbli biss għal dawk il-prodotti li ilhom awtorizzati mill-2016. Il-prodotti b’SPC sottomessi qabel l-1 ta’ Jannar 2016 se jkun fihom biss informazzjoni limitata fl-għodda ta’ tqabbil: l-ismijiet kummerċjali, iż-żona tas-suq, is-sustanza attiva (mingħajr konċentrazzjoni) u t-tip ta’ prodott.

Esporta r-riżultati

Tista’ tesporta r-riżultati tal-prodott bijoċidali għall-formati standard tas-sit web tal-ECHA (XLS, CSV u XML). Ir-riżultati esportati huma rranġati għal kull awtorizzazzjoni tal-prodott, eż. kull awtorizzazzjoni se tiġi ppreżentata f’ringiela individwali.

Il-kolonna “organiżmu fil-mira” fil-fajl esportat hija kombinazzjoni ta’ tliet oqsma: l-isem komuni, l-isem xjentifiku u l-istadju tal-iżvilupp, bħal: Adulti tal-far (Rattus norvegicus).

Jekk jogħġbok innota li minħabba limitazzjonijiet tekniċi bħalissa jidher biss numru limitat ta’ awtorizzazzjonijiet ikkanċellati u skaduti. Dawn se jiġu ppubblikati b’mod progressiv.

Lista li Tista’ Titniżżel (Estratt minn R4BP2)

Il-fajl li jista’ jitniżżel hawn taħt fih dawk l-awtorizzazzjonijiet tal-prodotti skont id-Direttiva 98/8/KE (id-Direttiva dwar il-Prodotti Bijoċidali) u r-Regolament (UE) Nru 528/2012 (ir-Regolament dwar il-Prodotti Bijoċidali) li ġew estratti mis-sistema tal-IT R4BP2 fl-1 ta’ Settembru 2013.

Innota li l-lista li tista’ titniżżel li tinsab hawn taħt hija bbażata fuq data disponibbli fis-sistema R4BP2 mill-1 ta’ Settembru 2013. Din id-data tista’ ma tkunx kompluta għalkollox, u lanqas kompletament aġġornata.

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Talogen 2

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PHASE VTA

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VITISEPSID

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Peracetic acid

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