+Člen 5
---+Article 5 1.
---+Article 5 2.

Člen 5

Člen 5

1.  Kadar določbe Skupnosti po začetku veljavnosti te direktive zahtevajo uporabo načel DLP za preskuse kemičnih proizvodov, države članice ne smejo na podlagi načel DLP prepovedati, omejiti ali ovirati dajanja kemičnih proizvodov na trg, če so načela, ki jih uporabljajo zadevni laboratoriji, v skladu z načeli, navedenimi v členu 1.

2.  Če država članica na podlagi podrobnih dokazil ugotovi, da uporaba načel DLP in preverjanje njihove uporabe pri preskusih kemičnih snovi kažeta, da snov, kljub temu da je bila preučena v skladu z zahtevami te direktive, ogroža človeka in okolje, lahko država članica začasno prepove ali postavi posebne pogoje za trženje te snovi na svojem ozemlju. O tem takoj obvesti Komisijo in druge države članice ter navede razloge za svojo odločitev.

Komisija se v šestih tednih posvetuje z zadevnimi državami članicami, nato da svoje mnenje in takoj sprejme ustrezne ukrepe.

▼M1

Komisija lahko sprejme izvedbene ukrepe za uvedbo potrebnih tehničnih prilagoditev te direktive.

Ti ukrepi, namenjeni spreminjanju nebistvenih določb te direktive, se sprejmejo v skladu z regulativnim postopkom s pregledom iz člena 4(2).

V primeru iz tretjega pododstavka lahko država članica, ki je sprejela zaščitne ukrepe, te ukrepe ohrani do začetka veljavnosti navedenih prilagoditev.

▼B

1. Pregled

,
Article 5 1.
Where Community provisions require application of the principles of GLP following the entry into force of this Directive for tests on chemical products, Member States may not, on grounds relating to the principles of GLP, prohibit, restrict or impede the placing on the market of chemical products if the principles applied by the laboratories concerned are in conformity with those mentioned in Article 1.
Article 5 2.
Should a Member State establish on the basis of detailed evidence that the application of the principles of GLP and the verification of their application for tests on chemical substances show that, although a chemical substance has been examined in accordance with the requirements of this Directive, it presents a danger to man and the environment, the Member State may provisionally prohibit or make subject to special conditions the marketing of that substance on its territory. It shall immediately inform the Commission and the other Member States thereof and give the grounds for its decision.

The Commission shall, within six weeks, consult the Member States concerned and then give its opinion and take suitable measures without delay.

The Commission may adopt implementing measures to introduce necessary technical adaptations of this Directive.

Those measures, designed to amend non-essential elements of this Directive, shall be adopted in accordance with the regulatory procedure with scrutiny referred to in Article 4(2).

In the case referred to in the third subparagraph, the Member State which adopted the safeguard measures may maintain them until the entry into force of those adaptations.

1.1 Sklici

1.2 Ugotovljene zahteve

1.3 Povezani standardi

2. Ugotovljene zahteve

Zahteve

3. Povezani standardi

Standardi
  • Builddate: 20.04.2009 00:00:00 -Doknr: CELEX:32004L0010
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