+Članak 6. Standardni postupak odobrenja
---+Article 6 1.
---+Article 6 2.
---+Article 6 2a.
---+Article 6 3.
---+Article 6 4.
---+Article 6 5.
---+Article 6 6.
---+Article 6 7.
---+Article 6 8.
---+Article 6 9.

Članak 6. Standardni postupak odobrenja

Članak 6.

Standardni postupak odobrenja

1.  Ne dovodeći u pitanje članak 5., svaka osoba mora, prije poduzimanja namjernog uvođenja GMO-a ili kombinacije GMO-a dostaviti prijavu nadležnom tijelu države članice na čijem državnom području će se provesti uvođenje.

2.  Prijava iz stavka 1. obuhvaća:

(a) 

tehnički dosje kojim se dostavljaju informacije utvrđene u Prilogu III. potrebne za provedbu procjene rizika za okoliš namjernog uvođenja GMO-a ili kombinacije GMO-a, posebno:

i. 

opće informacije uključujući informacije o osoblju i obuci;

ii. 

informacije vezane za GMO(-e);

iii. 

informacije vezane za uvjete uvođenja i potencijalni okoliš koji ih prima;

iv. 

informacije vezane za interakcije između GMO-a i okoliša;

v. 

plan praćenja u skladu s relevantnim dijelovima Priloga III. radi utvrđivanja učinaka GMO-a na zdravlje ljudi ili okoliš;

vi. 

informacije o kontroli, korektivnim mjerama, zbrinjavanju otpada i planovima hitnih mjera u hitnim slučajevima;

vii. 

sažetak dosjea;

(b) 

procjena rizika za okoliš i zaključci potrebni u Prilogu II. odjeljak D, zajedno s cjelokupnom literaturom i naznakama korištenih metoda.

▼M7

2.a  Prijava iz stavka 1. podnosi se u skladu sa standardnim formatima podataka, ako postoje prema pravu Unije.

▼B

3.  Podnositelj prijave može dostaviti dodatne podatke koje smatra relevantnima ili se pozvati na podatke ili rezultate iz prijava koje su prethodno predale druge osobe, pod uvjetom da informacije, podaci i rezultati nisu povjerljive prirode ili da su te druge osobe dale svoju pisanu suglasnost.

4.  Nadležno tijelo može prihvatiti da se uvođenja istoga GMO-a ili kombinacije GMO-a na istom mjestu ili na različitim mjestima u istu svrhu i u određenom roku mogu prijaviti u samo jednoj prijavi.

5.  Nadležno tijelo potvrđuje datum primitka prijave i nakon razmatranja, uzimajući u obzir eventualne primjedbe drugih država članica, u skladu s člankom 11., odgovara pisanim putem osobi koja je predala prijavu u roku od 90 dana od primitka prijave, i to na jedan od slijedećih načina:

(a) 

naznačivši da se uvjerilo da je prijava u skladu s ovom Direktivom i da se može krenuti s uvođenjem; ili

(b) 

naznačivši da uvođenje ne ispunjava uvjete iz ove Direktive i da se prijava stoga odbija.

6.  U svrhu računanja razdoblja od 90 dana iz stavka 5. ne uzimaju se u obzir razdoblja tijekom kojih nadležno tijelo:

(a) 

čeka daljnje podatke koje je zatražilo od podnositelja prijave; ili

(b) 

provodi javnu istragu ili savjetovanje u skladu s člankom 9.; ta javna rasprava ili savjetovanje ne produžuju razdoblje od 90 dana iz stavka 5. za više od 30 dana.

7.  Ako nadležno tijelo zatraži nove informacije, mora istodobno navesti razloge za to.

8.  Podnositelj prijave može nastaviti s uvođenjem tek kad dobije pisanu suglasnost nadležnog tijela i u skladu s eventualnim uvjetima utvrđenim u toj suglasnosti.

9.  Države članice osiguravaju da se ni jedan materijal dobiven iz GMO-a koji su namjerno uvedeni u skladu s dijelom B ne stavi na tržište ako nije u skladu s dijelom C.

1. Pregled

,
Article 6 1.
Without prejudice to Article 5, any person must, before undertaking a deliberate release of a GMO or of a combination of GMOs, submit a notification to the competent authority of the Member State within whose territory the release is to take place.
Article 6 2.

The notification referred to in paragraph 1 shall include:

(a) 

a technical dossier supplying the information specified in Annex III necessary for carrying out the environmental risk assessment of the deliberate release of a GMO or combination of GMOs, in particular:

(i) 

general information including information on personnel and training,

(ii) 

information relating to the GMO(s),

(iii) 

information relating to the conditions of release and the potential receiving environment,

(iv) 

information on the interactions between the GMO(s) and the environment,

(v) 

a plan for monitoring in accordance with the relevant parts of Annex III in order to identify effects of the GMO(s) on human health or the environment,

(vi) 

information on control, remediation methods, waste treatment and emergency response plans,

(vii) 

a summary of the dossier;

(b) 

the environmental risk assessment and the conclusions required in Annex II, section D, together with any bibliographic reference and indications of the methods used.
Article 6 2a.
The notification referred to in paragraph 1 shall be submitted in accordance with standard data formats, where they exist under Union law.
Article 6 3.
The notifier may refer to data or results from notifications previously submitted by other notifiers, provided that the information, data and results are non confidential or these notifiers have given their agreement in writing, or may submit additional information he considers relevant.
Article 6 4.
The competent authority may accept that releases of the same GMO or of a combination of GMOs on the same site or on different sites for the same purpose and within a defined period may be notified in a single notification.
Article 6 5.

The competent authority shall acknowledge the date of receipt of the notification and, having considered, where appropriate, any observations by other Member States made in accordance with Article 11, shall respond in writing to the notifier within 90 days of receipt of the notification by either:

(a) 

indicating that it is satisfied that the notification is in compliance with this Directive and that the release may proceed; or

(b) 

indicating that the release does not fulfil the conditions of this Directive and that notification is therefore rejected.
Article 6 6.

For the purpose of calculating the 90 day period referred to in paragraph 5, no account shall be taken of any periods of time during which the competent authority:

(a) 

is awaiting further information which it may have requested from the notifier, or

(b) 

is carrying out a public inquiry or consultation in accordance with Article 9; this public inquiry or consultation shall not prolong the 90 day period referred to in paragraph 5 by more than 30 days.
Article 6 7.
If the competent authority requests new information it must simultaneously give its reasons for so doing.
Article 6 8.
The notifier may proceed with the release only when he has received the written consent of the competent authority, and in conformity with any conditions required in this consent.
Article 6 9.
Member States shall ensure that no material derived from GMOs which are deliberately released in accordance with part B is placed on the market, unless in accordance with part C.

1.1 Reference

1.2 Utvrđeni zahtjevi

1.3 Povezani standardi

2. Utvrđeni zahtjevi

Zahtjevi

3. Povezani standardi

Standardi
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