+Artikolu 7 Proċeduri differenzjati
---+Article 7 1.
---+Article 7 2.
---+Article 7 3.
---+Article 7 4.
---+Article 7 5.
---+Article 7 6.
---+Article 7 7.

Artikolu 7 Proċeduri differenzjati

Artikolu 7

Proċeduri differenzjati

1.  Jekk inkisbet esperjenza suffiċjenti minn rilaxxi ta' ċerti GMOs f'ċerti ekosistemi u l-GMOs konċernati josservaw il-kriterji stabbiliti fl-Anness V, awtorità kompetenti tista' tagħti lil Kummissjoni proposta raġjunata għal applikazzjoni ta' proċeduri differenti għal ċerti tipi ta' GMOs.

2.  Fuq inizjattiva tagħha jew l-aktar tard 30 ġurnata wara riċevuta tal-proposta mill-awtorità kompetenti, il-Kummissjoni għandha,

(a) 

twassal il-proposta lill-awtoritajiet kompetenti, li jistgħu, fi żmien 60 ġurnata, jippreżentaw osservazzjonijiet u fl-istess ħin;

(b) 

tagħmel disponibbli l-proposta lill-pubbliku li jista', fi żmien 60 ġurnata jagħmel kummenti; u

(ċ) 

jikkonsulta' il Kumitat(i) Xjentifiku rilevanti li jista, fi żmien 60 ġurnata jagħti opinjoni.

3.  Deċiżjoni għandha tittieħed fuq kull proposta skond il-proċedura stabbilita fl-Artikolu 30(2). Din id-Deċiżjoni għandha tistabbilixxi l-ammont minimu ta' informazzjoni teknika mill-Anness III neċessarja biex tevalwa kull riskju previst mir-rilaxx, in partikolari:

(a) 

informazjoni dwar GMO(s);

(b) 

informazzjoni dwar il-kondizzjonijiet ta' rilaxx u l-ambjent potenzjali li qiegħed jirċievi;

(ċ) 

informazzjoni dwar interazzjonijiet bejn GMO(s) u l-ambjent;

(d) 

stima ta' riskju ambjentali.

4.  Din id-Deċiżjoni għandha tittieħed fi żmien 90 ġurnata mill-proposta tal-Kummissjoni jew ta' rċevuta tal-proposta ta' l-awtorità kompetenti. Dan il-perijodu ta' 90 ġurnata ma jiħux akkont tal-perijodu ta' żmien li matulu l-Kummissjoni qed tistenna l-osservazzjonijiet ta' l-awtoritajiet kompetenti, il-kummenti tal-pubbliku jew l-opinjoni tal-Kumitati Xjentifiċi, kif provvdut fil-paragrafu 2.

5.  Id-Deċiżjoni li ttieħdet skond il-paragrafi 3 u 4 tipprovdi li n-notifikant jista' jipproċedi bir-rilaxx biss meta jirċievi il-kunsens bil-miktub ta' l-awtorità kompetenti. In-notifikant jipproċedi bir-rilaxx in konformità ma' kwalunkwe kondizzjoni rikjesta f'dan il-kunsens.

Id-Deċiżjoni li tittieħed skond il-paragrafi 3 u 4 tista' tipprovdi li r-rilaxx ta' GMO jew tagħqid ta' GMOs fuq l-istess sit jew fuq siti differenti għall-istess skop u f'perijodu definit jistgħu jiġu notifikati b'notifika waħda.

6.  Mingħajr preġudizzju għall-paragrafi 1 sa 5, id-Deċiżjoni TAL-KUMMISSJONI 94/730/KE tal-4 ta' Novembru 1994 li tistipula proċeduri simplifikati dwar rilaxx intenzjonat fl-ambjent ta' pjanti ġenetikament modifikati skond l-artikolu 6(5) tad-Direttiva tal-Kunsill 90/220/KEE ( 2 ) tkompli tapplika.

7.  Meta Stat Membru jiddeċiedi li jagħmel użu jew le ta' proċedura stabbilita f'deċiżjoni li ttieħdet skond il-paragrafi 3 u 4 għar-rilaxxament ta' GMOs fit-territorju tiegħu, għandu jinforma lil Kummissjoni b'dan.

1. Ħarsa ġenerali

,
Titlu Regolamentazzjoni
Article 7 1.
If sufficient experience has been obtained of releases of certain GMOs in certain ecosystems and the GMOs concerned meet the criteria set out in Annex V, a competent authority may submit to the Commission a reasoned proposal for the application of differentiated procedures to such types of GMOs.
Article 7 2.

Following its own initiative or at the latest 30 days following the receipt of a competent authority's proposal, the Commission shall,

(a) 

forward the proposal to the competent authorities, which may, within 60 days, present observations and at the same time;

(b) 

make available the proposal to the public which may, within 60 days, make comments; and

(c) 

consult the relevant Scientific Committee(s) which may, within 60 days give an opinion.

Article 7 3.

A decision shall be taken on each proposal in accordance with the procedure laid down in Article 30(2). This decision shall establish the minimum amount of technical information from Annex III necessary for evaluating any foreseeable risks from the release, in particular:

(a) 

information relating to the GMO(s);

(b) 

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

(c) 

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

(d) 

the environmental risk assessment.

Article 7 4.
This decision shall be taken within 90 days of the date of the Commission's proposal or of receipt of the competent authority's proposal. This 90 day period shall not take into account the period of time during which the Commission is awaiting the observations of competent authorities, the comments of the public or the opinion of Scientific Committees, as provided for in paragraph 2.
Article 7 5.
The decision taken under paragraphs 3 and 4 shall provide that the notifier may proceed with the release only when he has received the written consent of the competent authority. The notifier shall proceed with the release in conformity with any conditions required in this consent.

The decision taken under paragraphs 3 and 4 may provide that releases of a 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 7 6.
Without prejudice to paragraphs 1 to 5, Commission Decision 94/730/EC of 4 November 1994 establishing simplified procedures concerning the deliberate release into the environment of genetically modified plants pursuant to Article 6(5) of Council Directive 90/220/EEC ( 2 ) shall continue to apply.
Article 7 7.
Where a Member State decides to make use or not of a procedure established in a decision taken in accordance with paragraphs 3 and 4 for releases of GMOs within its territory, it shall inform the Commission thereof.

1.1 Referenzi

1.2 Rekwiżiti identifikati

1.3 Standards relatati

2. Rekwiżiti identifikati

Rekwiżiti
Sors Rekwiżit

3. Standards relatati

Standards
Sors Rekwiżit
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