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. 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. 3. This Directive does not concern the interpretation and evaluation of test results.