+Artikolu 3 3
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Artikolu 3 3
3. B’deroga mill-paragrafu 2, il-pjattaforma komuni tad-data għandha tipprovdi aċċess għad-data dwar sustanzi kimiċi relatata ma’ prodotti mediċinali tal-bniedem u veterinarji bħala parti mill-implimentazzjoni tal-atti legali tal-Unjoni elenkati fl-Anness I, il-Parti 2, unikament jekk tali data:
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(b)
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għandha x’taqsam ma’ sustanzi attivi:
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(i)
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li huma soġġetti għal proċessi regolatorji skont atti legali oħra tal-Unjoni elenkati fl-Anness I, il-Parti 1; jew
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(ii)
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li għandhom proprjetajiet persistenti, bijoakkumulattivi u tossiċi partikolari; jew
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(iii)
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li għalihom ġie identifikat livell għoli ta’ residwi fl-ambjent; u
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(c)
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taqa’ f’tal-anqas waħda mill-kategoriji li ġejjin:
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(i)
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data mhux klinika dwar is-sikurezza, inkluża data relatata mal-valutazzjonijiet tar-riskju ambjentali, ikkompilata skont id-Direttiva 2001/83/KE tal-Parlament Ewropew u tal-Kunsill (17) u r-Regolament (KE) Nru 726/2004 tal-Parlament Ewropew u tal-Kunsill (18); jew
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(ii)
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data relatata mal-valutazzjonijiet tar-riskju ambjentali, ikkompilata skont ir-Regolament (UE) 2019/6 tal-Parlament Ewropew u tal-Kunsill (19);)jew
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(iii)
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il-livelli massimi ta’ residwu u d-data li huma derivati minnha, ikkompilata skont ir-Regolament (KE) Nru 470/2009 tal-Parlament Ewropew u tal-Kunsill (20).
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1. Ħarsa ġenerali
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Regolamentazzjoni |
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1.1 Referenzi
1.2 Rekwiżiti identifikati
1.3 Standards relatati
2. Rekwiżiti identifikati
3. Standards relatati
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