+Članak 1.
---+Article 1 1.
---+Article 1 2.
---+Article 1 3.

Članak 1.

Članak 1.

1.  Ova se Direktiva primjenjuje na nadzor i provjeru organizacijskih metoda i uvjeta pod kojima se, u skladu s pravilima i propisima, planiraju, izvode, bilježe i izvješćuju laboratorijska ispitivanja za neklinička testiranja, za sve kemijske proizvode (npr. kozmetička sredstva, industrijske kemijske proizvode, lijekove, dodatke hrani, dodatke stočnoj hrani, pesticide), kako bi se ocijenio učinak takvih proizvoda na čovjeka, životinje i okoliš.

2.  Za potrebe ove Direktive „dobra laboratorijska praksa” (DLP) znači laboratorijsku praksu u skladu s načelima iz Direktive 2004/10/EZ.

3.  Ova se Direktiva ne odnosi na tumačenje i ocjenu rezultata ispitivanja.

1. Pregled

,
Article 1 1.
This Directive shall apply to the inspection and verification of the organisational processes and the conditions under which laboratory studies are planned, performed, recorded and reported for the non-clinical testing, carried out in accordance with the rules and regulations, of all chemicals (e.g. cosmetics, industrial chemicals, medicinal products, food additives, animal feed additives, pesticides) in order to assess the effect of such products on man, animals and the environment.
Article 1 2.
For the purposes of this Directive, ‘good laboratory practice’ (GLP), shall mean laboratory practice conducted in accordance with the principles set out in Directive 2004/10/EC.
Article 1 3.
This Directive does not concern the interpretation and evaluation of test results.

1.1 Reference

1.2 Utvrđeni zahtjevi

1.3 Povezani standardi

2. Utvrđeni zahtjevi

Zahtjevi

3. Povezani standardi

Standardi
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