+Artikolu 17 Tiġdid ta' kunsens
---+Article 17 1.
---+Article 17 2.
---+Article 17 3.
---+Article 17 4.
---+Article 17 5.
---+Article 17 6.
---+Article 17 7.
---+Article 17 8.
---+Article 17 9.

Artikolu 17 Tiġdid ta' kunsens

Artikolu 17

Tiġdid ta' kunsens

1.  B'deroga mill-Artikoli 13, 14 u 15, il-proċedura stabbilita fil-paragrafi 2 sa 9 tiġi applikata għat-tiġdid ta':

(a) 

kunsensi li ingħataw skond il-Parti Ċ; u

(b) 

qabel is-17 ta' Ottubru 2006 ta' kunsensi li ingħataw skond id-Direttiva 90/220/KEE għat-tpoġġija fis-suq ta' GMOs bħal jew fi prodotti qabel is-17 ta' Ottubru 2002,

2.  Sa disa' xhur massimu qabel li jiskadi l-kunsens, għal kunsensi riferiti fil-paragrafu 1(a), u qabel is-17 ta' Ottubru 2006, għal kunsensi riferiti fil-paragrafu 1(b), in-notifikant skond dan l-Artikolu għandu jagħti notifika lill-awtorità kompetenti li rċievet in-notifika oriġinali, li jkun fiha:

(a) 

kopja tal-kunsens għat-tpoġġija fis-suq ta' GMOs;

(b) 

rapport fuq ir-riżultati ta' sorveljanza li sar skond l-Artikolu 20. Fil-każ ta' kunsensi riferiti fil-paragrafu 1(b), dan ir-rapport għandu jiġi mogħti meta issir is-sorveljanza;

(ċ) 

kwalunkwe informazzjoni oħra ġdida li saret disponibbli dwar ir-riskji tal-prodott lis-saħħa tal-bniedem u/jew l-ambjent; u

(d) 

kif xieraq, proposta biex temenda jew tikkomplimenta l-kondizzjonijiet tal-kunsens oriġinali, inter alia l-kondizzjonijiet dwar sorveljar futur u limitazzjoni ta' żmien tal-kunsens.

L-awtortità kompetenti għandha tgħarraf id-data meta tirċievi in-notifika u meta notifika ssir skond dan il-paragrafu mingħajr dewmien tibgħat kopja tan-notifika u r-rapport ta' stima lill-Kummissjoni, li, fi żmien 30 ġurnata minn meta tirċievih, tibgħathom lil awtoritajiet kompetenti ta' l-Istati Membri l-oħra. Tibgħat ukoll ir-rapport ta' stima tagħha lin-notifikant.

3.  Ir-rapport ta'stima għandu jindika jekk:

(a) 

il-GMO(s) għandhomx jibqgħu fis-suq u b' liema kondizzjonijiet; jew

(b) 

il-GMO(s) m'għandhomx jibqgħu fis-suq.

4.  L-awtoritajiet kompetenti l-oħra jew il-Kummissjoni tista' titlob għal aktar informazzjoni, tagħmel kummenti, jew tippreżenta oġġezzjonijiet raġjunati fi żmien 60 ġurnata mid-data ta' ċirkolazzjoni tar-rapport ta' stima.

5.  Il-kummenti kollha, oġġezzjonijiet raġjunati u tweġibiet jintbagħtu lill-Kummissjoni li immedjatament għandha tiċċirkolhom lil awtoritjiet kompetenti kollha.

6.  Fil-każ tal-paragrafu 3(a) u fl-assenza ta' xi oġġezzjoni raġjunata minn Stat Membru jew mill-Kummissjoni fi żmien 60 ġurnata mid-data ta' ċirkolazzjoni tar-rapport ta' stima, l-awtorità kompetenti li ppreparat ir-rapport għandha tibgħat lin-notifikant id-deċiżjoni finali bil-miktub u tinforma lill-Istati Membri l-oħra u lill-Kummissjoni b'dan fi żmien 30 ġurnata. Il-validità tal-kunsens m'għandhiex, bħala regola ġenerali, teċċedi għaxar snin u tista' tiġi limitata jew estiża kif xieraq għal raġunijiet speċifiċi.

7.  L-awtoritajiet kompetenti u l-Kummisjoni jistgħu jiddiskutu xi kwistjonijiet li għadu ma ntlaħaqx ftehim dwarhom, bil-għan li jilħqu ftehim fi żmien 75 ġurnata mid-data ta' ċirkolazzjoni ta' rapport ta' stima.

8.  Jekk kwistjonijiet mhux solvuti jiġu solvuti f'perijodu ta' 75 ġurnata riferiti fil-paragrafu 7, l-awtorità kompetenti li ppreparat ir-rapport għandha tibgħat lin-notifikant id-deċiżjoni finali tagħha bil-miktub, u tinforma lill-Istati Membri l-oħra u lill-Kummissjoni b'dan fi żmien 30 ġurnata. Il-validità tal-kunsens tista' tiġi limitata kif xieraq.

9.  Wara notifika għat-tiġdid ta' kunsens skond il-paragrafu 2, in-notifikant jista' jibqa' jpoġġi GMOs fis-suq skond il-kondizzjonijiet speċifikati f'dak il-kunsens sakemm tittieħed deċiżjoni finali fuq in-notifika.

1. Ħarsa ġenerali

,
Titlu Regolamentazzjoni
Article 17 1.

By way of derogation from Articles 13, 14 and 15, the procedure set out in paragraphs 2 to 9 shall be applied to the renewal of:

(a) 

consents granted under part C; and

(b) 

before 17 October 2006 of consents granted under Directive 90/220/EEC for placing on the market of GMOs as or in products before 17 October 2002,

Article 17 2.

At the latest nine months before the expiry of the consent, for the consents referred to in paragraph 1(a), and before 17 October 2006, for the consents referred to in paragraph 1(b), the notifier under this Article shall submit a notification to the competent authority which received the original notification, which shall contain:

(a) 

a copy of the consent to the placing on the market of the GMOs;

(b) 

a report on the results of the monitoring which was carried out according to Article 20. In the case of consents referred to in paragraph 1(b), this report shall be submitted when the monitoring was carried out;

(c) 

any other new information which has become available with regard to the risks of the product to human health and/or the environment; and

(d) 

as appropriate, a proposal for amending or complementing the conditions of the original consent, inter alia the conditions concerning future monitoring and the time limitation of the consent.

The competent authority shall acknowledge the date of receipt of the notification and when the notification is in accordance with this paragraph it shall without delay forward a copy of the notification and its assessment report to the Commission, which shall, within 30 days of their receipt, forward them to the competent authorities of the other Member States. It shall also send its assessment report to the notifier.

Article 17 3.

The assessment report shall indicate whether:

(a) 

the GMO(s) should remain on the market and under which conditions; or

(b) 

the GMO(s) should not remain on the market.

Article 17 4.
The other competent authorities or the Commission may ask for further information, make comments, or present reasoned objections within a period of 60 days from the date of circulation of the assessment report.
Article 17 5.
All comments, reasoned objections and replies shall be forwarded to the Commission which shall immediately circulate them to all competent authorities.
Article 17 6.
In the case of paragraph 3(a) and in the absence of any reasoned objection from a Member State or the Commission within 60 days from the date of circulation of the assessment report, the competent authority which prepared the report shall transmit to the notifier the final decision in writing and shall inform the other Member States and the Commission thereof within 30 days. The validity of the consent should not, as a general rule, exceed ten years and may be limited or extended as appropriate for specific reasons.
Article 17 7.
The competent authorities and the Commission may discuss any outstanding issues with the aim of arriving at an agreement within 75 days from the date of circulation of the assessment report.
Article 17 8.
If outstanding issues are resolved within the 75 day period referred to in paragraph 7, the competent authority which prepared the report shall transmit to the notifier its final decision in writing and shall inform the other Member States and the Commission thereof within 30 days. The validity of the consent may be limited as appropriate.
Article 17 9.
Following a notification for the renewal of a consent in accordance with paragraph 2, the notifier may continue to place the GMOs on the market under the conditions specified in that consent until a final decision has been taken on the notification.

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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