+Članak 19. Suglasnost
---+Article 19 1.
---+Article 19 2.
---+Article 19 3.
---+Article 19 4.

Članak 19. Suglasnost

Članak 19.

Suglasnost

1.  Ne dovodeći u pitanje zahtjeve na temelju drugog zakonodavstva Zajednice, samo ako se za stavljanje GMO-a na tržište kao proizvodâ ili u sastavu proizvodâ daje pisana suglasnost, taj se proizvod može koristiti bez daljnje prijave u Zajednici pod uvjetom da se strogo pridržava posebnih uvjeta uporabe i okoliša i/ili zemljopisnih područja utvrđenih u tim uvjetima.

2.  Podnositelj prijave može nastaviti sa stavljanjem na tržište tek kada dobije pisanu suglasnost nadležnog tijela u skladu s člancima 15., 17. i 18. te u skladu sa svim uvjetima traženim u toj suglasnosti.

3.  U pisanoj suglasnosti iz članaka 15., 17. i 18. u svakom se slučaju izričito utvrđuje:

(a) 

opseg suglasnosti, uključujući identitet GMO-a koji se stavljaju na tržište kao proizvodi ili sastojci proizvodâ, i njihova jedinstvena oznaka;

(b) 

rok valjanosti suglasnosti;

(c) 

uvjete za stavljanje proizvoda na tržište, uključujući sve posebne uvjete uporabe, rukovanja i pakiranja GMO-a kao proizvodâ ili sastojka proizvodâ, te uvjete za zaštitu pojedinih ekosustava/okoliša i/ili zemljopisnih područja;

(d) 

da, ne dovodeći u pitanje članak 25., podnositelj prijave na zahtjev dostavlja kontrolne uzorke na raspolaganje nadležnom tijelu;

(e) 

zahtjeve u vezi s označivanjem, u skladu sa zahtjevima utvrđenim u Prilogu IV. U oznaci se jasno mora navesti da je GMO prisutan. Riječi „Ovaj proizvod sadrži genetski modificirane organizme” moraju biti navedene na oznaci ili u dokumentu koji prati proizvod ili druge proizvode koji sadrže GMO-e;

(f) 

zahtjeve u vezi s praćenjem u skladu s Prilogom VII., uključujući obveze izvješćivanja Komisije i nadležnih tijela, rok za plan praćenja i, prema potrebi, sve obveze osobe koja prodaje proizvod ili korisnika proizvoda, između ostalog u slučaju uzgojenoga GMO-a, u vezi s razinom informacija koje se smatraju primjerenim na određenoj lokaciji.

4.  Države članice poduzimaju sve potrebne mjere kako bi osigurale da se pisana suglasnost i odluka iz članka 18., prema potrebi, stave na raspolaganje javnosti i da su uvjeti navedeni u pisanoj suglasnosti i odluci ispunjeni.

1. Pregled

,
Article 19 1.
Without prejudice to requirements under other Community legislation, only if a written consent has been given for the placing on the market of a GMO as or in a product may that product be used without further notification throughout the Community in so far as the specific conditions of use and the environments and/or geographical areas stipulated in these conditions are strictly adhered to.
Article 19 2.
The notifier may proceed with the placing on the market only when he has received the written consent of the competent authority in accordance with Articles 15, 17 and 18, and in conformity with any conditions required in that consent.
Article 19 3.

The written consent referred to in Articles 15, 17 and 18 shall, in all cases, explicitly specify:

(a) 

the scope of the consent, including the identity of the GMO(s) to be placed on the market as or in products, and their unique identifier;

(b) 

the period of validity of the consent;

(c) 

the conditions for the placing on the market of the product, including any specific condition of use, handling and packaging of the GMO(s) as or in products, and conditions for the protection of particular ecosystems/environments and/or geographical areas;

(d) 

that, without prejudice to Article 25, the notifier shall make control samples available to the competent authority on request;

(e) 

the labelling requirements, in compliance with the requirements laid down in Annex IV. The labelling shall clearly state that a GMO is present. The words ‘This product contains genetically modified organisms’ shall appear either on a label or in a document accompanying the product or other products containing the GMO(s);

(f) 

monitoring requirements in accordance with Annex VII, including obligations to report to the Commission and competent authorities, the time period of the monitoring plan and, where appropriate, any obligations on any person selling the product or any user of it, inter alia, in the case of GMOs grown, concerning a level of information deemed appropriate on their location.
Article 19 4.
Member States shall take all necessary measures to ensure that the written consent and the decision referred to in Article 18, where applicable, are made accessible to the public and that the conditions specified in the written consent and the decision, where applicable, are complied with.

1.1 Reference

1.2 Utvrđeni zahtjevi

1.3 Povezani standardi

2. Utvrđeni zahtjevi

Zahtjevi

3. Povezani standardi

Standardi
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