+Članak 23. Zaštitna klauzula
---+Article 23 1.
---+Article 23 2.

Članak 23. Zaštitna klauzula

Članak 23.

Zaštitna klauzula

1.  Kada država članica, na temelju dostupnosti novih ili dodatnih informacija stavljenih na raspolaganje od datuma suglasnosti koje utječu na procjenu rizika za okoliš ili ponovnu procjenu postojećih informacija na temelju novih ili dodatnih znanstvenih spoznaja, ima detaljne osnove da može smatrati da GMO kao proizvod ili sastojak proizvoda koji je na primjeren način prijavljen i za koji je dobivena pisana suglasnost na temelju ove Direktive, predstavlja rizik za zdravlje ljudi ili okoliš, ta država članica može na svojem državnom području privremeno ograničiti ili zabraniti uporabu i/ili prodaju toga GMO-a kao proizvoda ili sastojka proizvoda.

Država članica osigurava da se u slučaju ozbiljnog rizika primijene hitne mjere, poput suspenzije ili prestanka stavljanja na tržište, uključujući i obavješćivanje javnosti.

Država članica odmah izvješćuje Komisiju i druge države članice o mjerama poduzetima na temelju ovog članka i obrazlaže svoju odluku, dostavljajući svoje preispitivanje procjene rizika za okoliš u kojoj navodi treba li izmijeniti uvjete suglasnosti i kako, ili treba ukinuti suglasnost i, prema okolnostima, nove ili dodatne informacije na kojima se njezina odluka temelji.

▼M3

2.  Odluka o mjeri koju poduzima ta država članica donosi se u skladu s regulatornim postupkom iz članka 30. stavka 2. u roku od 60 dana od datuma primitka informacije koju je dostavila država članica. U svrhu računanja roka od 60 dana ne uzima se u obzir razdoblje u kojem Komisija čeka dodatne informacije koje je zatražila od podnositelja prijave ili u kojem traži mišljenje Znanstvenog(-ih) odbora s kojim(-a) se savjetuje. Vrijeme tijekom kojeg Komisija čeka mišljenje Znanstvenog(-ih) odbora s kojim(-a) se savjetuje ne prelazi 60 dana.

Jednako tako, u obzir se ne uzima ni vrijeme koje Vijeće treba kako bi djelovalo u skladu s regulatornim postupkom iz članka 30. stavka 2.

▼B

1. Pregled

,
Article 23 1.
Where a Member State, as a result of new or additional information made available since the date of the consent and affecting the environmental risk assessment or reassessment of existing information on the basis of new or additional scientific knowledge, has detailed grounds for considering that a GMO as or in a product which has been properly notified and has received written consent under this Directive constitutes a risk to human health or the environment, that Member State may provisionally restrict or prohibit the use and/or sale of that GMO as or in a product on its territory.

The Member State shall ensure that in the event of a severe risk, emergency measures, such as suspension or termination of the placing on the market, shall be applied, including information to the public.

The Member State shall immediately inform the Commission and the other Member States of actions taken under this Article and give reasons for its decision, supplying its review of the environmental risk assessment, indicating whether and how the conditions of the consent should be amended or the consent should be terminated, and, where appropriate, the new or additional information on which its decision is based.
Article 23 2.
Within 60 days of the date of receipt of the information transmitted by the Member State, a decision shall be taken on the measure taken by that Member State in accordance with the regulatory procedure referred to in Article 30(2). For the purpose of calculating the 60-day period, any period of time during which the Commission is awaiting further information which it may have requested from the notifier or is seeking the opinion of the Scientific Committee or Committees which has or have been consulted shall not be taken into account. The period of time during which the Commission is awaiting the opinion of the Scientific Committee or Committees consulted shall not exceed 60 days.

Likewise, the period of time the Council takes to act in accordance with the regulatory procedure referred to in Article 30(2) shall not be taken into account.

1.1 Reference

1.2 Utvrđeni zahtjevi

1.3 Povezani standardi

2. Utvrđeni zahtjevi

Zahtjevi

3. Povezani standardi

Standardi
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