+Artikolu 16 Kriterji u informazzjoni għal GMOs speċifikati
---+Article 16 1.
---+Article 16 2.
---+Article 16 3.

Artikolu 16 Kriterji u informazzjoni għal GMOs speċifikati

Artikolu 16

Kriterji u informazzjoni għal GMOs speċifikati

1.  Awtorità kompetenti, jew il-Kummissjoni fuq inizjattiva tagħha, tista' tagħmel proposta fuq kriterji u rekwiżiti ta' informazzjoni li għandhom jiġu osservati min-notifika, b'deroga mill-Artikolu 13, għat-tpoġġija fis-suq ta' ċerti tipi ta' GMOs bħal jew fi prodotti.

▼M3

2.   ►M6  Il-Kummissjoni għandha s-setgħa li tadotta atti delegati f’konformità mal-Artikolu 29a sabiex tissupplimenta din id-Direttiva billi tistabbilixxi l-kriterji u r-rekwiżiti tal-informazzjoni msemmija fil-paragrafu 1, kif ukoll kwalunkwe rekwiżit xieraq għal sommarju tad-dossier, wara konsultazzjoni tal-Kumitat Xjentifiku rilevanti. Il-kriterji u r-rekwiżiti ta’ informazzjoni għandhom ikunu tali li jassiguraw livell għoli ta’ sigurtà lis-saħħa tal-bniedem u l-ambjent u jkunu bbażati fuq evidenza xjentifika disponibbli fuq din is-sigurtà u mill-esperjenza miksuba mir-rilaxx ta’ GMOs komparabbli. ◄

Ir-rekwiżiti stabbiliti fl-Artikolu 13(2) għandhom jiġu mibdula b’dawk adottati skond l-ewwel subparagrafu, u għandha tapplika l-proċedura stabbilita fl-Artikolu 13(3), (4), (5) u (6) u l-Artikoli 14 u 15.

▼M6

3.  Qabel ma tadotta atti delegati skont il-paragrafu 2, il-Kummissjoni għandha tagħmel il-proposta disponibbli għall-pubbliku. Il-pubbliku jista’ jagħmel kummenti lill-Kummissjoni fi żmien 60 jum. Il-Kummissjoni għandha tibgħat kwalunkwe dokumenti bħal dawn, flimkien ma’ analiżi, lill-esperti msemmija fl-Artikolu 29a(4).

▼B

1. Ħarsa ġenerali

,
Article 16 1.
A competent authority, or the Commission on its own initiative, may make a proposal on criteria and information requirements to be met for the notification, by way of derogation from Article 13, for the placing on the market of certain types of GMOs as or in products.
Article 16 2.
►M6  The Commission is empowered to adopt delegated acts in accordance with Article 29a in order to supplement this Directive by establishing the criteria and information requirements referred to in paragraph 1, as well as any appropriate requirements for a summary of the dossier, after consultation of the relevant Scientific Committee. The criteria and information requirements shall be such as to ensure a high level of safety of human health and the environment and shall be based on the available scientific evidence concerning such safety and on experience gained from the release of comparable GMOs. ◄

The requirements set out in Article 13(2) shall be replaced by those adopted in accordance with the first subparagraph, and the procedure set out in Article 13(3), (4), (5) and (6) and Articles 14 and 15 shall apply.
Article 16 3.
Before adopting delegated acts pursuant to paragraph 2, the Commission shall make the proposal available to the public. The public may make comments to the Commission within 60 days. The Commission shall forward any such comments, together with an analysis, to the experts referred to in Article 29a(4).

1.1 Referenzi

1.2 Rekwiżiti identifikati

1.3 Standards relatati

2. Rekwiżiti identifikati

Rekwiżiti

3. Standards relatati

Standards
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