Produits pharmaceutiques pour animaux

Tierarzneimittel
Tierarzneimittel
Tierarzneimittel
 

LAUS supports you in conducting the environmental risk assessment (ERA) for the registration of your veterinary medicinal product in accordance with the requirements of the European Medicines Agency (EMEA). The test consists of two phases. Phase 2 is, however, only required if certain criteria can not be met in Phase 1.

Together with our partner laboratories, we offer you the complete range of tests according to the principles of Good Laboratory Practice (GLP) with the following services:

Environmental Risk Assessment (acc. CVMP/ERA/418282/2005-Ref.1):

Phase II: Tier A

  • Physico-chemical Properties
  • Environmental Fate
  • Aquatic Ecotoxicology
  • Terrestrial Ecotoxicology

Phase II: Tier B

(Depending on the results of the studies from Tier A)

  • Environmental Fate
  • Aquatic Ecotoxicology
  • Terrestrial Ecotoxicology