+Artikolu 28 Konsultazzjoni ta' Kumitat (i) Xjentifiku
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Artikolu 28 Konsultazzjoni ta' Kumitat (i) Xjentifiku

Artikolu 28

Konsultazzjoni ta' Kumitat (i) Xjentifiku

1.  F'każijiet fejn jitqajjmu mill-awtorità kompetenti jew mill-Kummissjoni oġġezzjoni dwar riskji ta' GMOs għas-saħħa tal-bniedem jew lil ambjent u miżmum skond l-Artikoli 15(1), 17(4), 20(3) jew 23, jew fejn ir-rapport ta' stima riferit fl-Artikolu 14 jindika li l-GMO m'għandux jitpoġġa fis-suq, il-Kumitat rilevanti Xjentifiku jiġu konsultati mill-Kummissjoni, fuq inizjattiva tagħhom jew fuq talba ta' Stat Membru, fuq oġġezzjoni.

2.  Il-Kumitat(i) rilevanti Xjentifiku jista' wkoll jiġi konsultat mill-Kummissjoni, fuq inizjattiva tagħha jew fuq talba ta' Stat Membru, fuq kwalunkwe kwistjoni skond din id-Direttiva li jista' jkollha effett ħażin fuq is-saħħa tal-bniedem u l-ambjent.

3.  Il-proċeduri amministrattivi stabbiliti f'din id-direttiva ma jiġux affetwati minn paragrafu 2.

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4.  Meta l-Kumitat Xjentifiku rilevanti jiġi kkonsultat skont il-paragrafu 1 ta' dan l-Artikolu, dan għandu mingħajr dewmien jagħmel pubblika n-notifika, l-informazzjoni ta' appoġġ rilevanti u kwalunkwe informazzjoni supplimentari fornita min-notifikatur, kif ukoll l-opinjonijiet xjentifiċi tiegħu, bl-eċċezzjoni ta' kwalunkwe informazzjoni li tkun ingħatat trattament kunfidenzjali mill-awtorità kompetenti b'konformità mal-Artikolu 25.

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1. Ħarsa ġenerali

,
Article 28 1.
In cases where an objection as regards the risks of GMOs to human health or to the environment is raised by a competent authority or the Commission and maintained in accordance with Article 15(1), 17(4), 20(3) or 23, or where the assessment report referred to in Article 14 indicates that the GMO should not be placed on the market, the relevant Scientific Committee(s) shall be consulted by the Commission, on its own initiative or at the request of a Member State, on the objection.
Article 28 2.
The relevant Scientific Committee(s) may also be consulted by the Commission, on its own initiative or at the request of a Member State, on any matter under this Directive that may have an adverse effect on human health and the environment.
Article 28 3.
The administrative procedures laid down in this Directive shall not be affected by paragraph 2.
Article 28 4.
Where the relevant Scientific Committee is consulted in accordance with paragraph 1 of this Article, it shall make public without delay the notification, relevant supporting information and any supplementary information supplied by the notifier, as well as its scientific opinions, with the exception of any information to which the competent authority has granted confidential treatment in accordance with Article 25.

1.1 Referenzi

1.2 Rekwiżiti identifikati

1.3 Standards relatati

2. Rekwiżiti identifikati

Rekwiżiti

3. Standards relatati

Standards
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