LAUS GmbH uses state-of-the-art equipment for scientifically advanced studies. Examinations which we don’t perform ourselves, are passed on to accreditated and/or certified partners only.

Our quality assurance system was developed and established by ourselves, ensuring timely updates, continuity and transparency. Participation in international meetings and workshops for quality assurance are self-evident.

Our next goal is the realization of FDA Rule 21 CFR 11 in all our laboratories in order to be able to provide our customers the paperless registration procedure at the FDA.

GLP – Good Laboratory Practice

• Category 1
  Studies for the determination of physico-chemical properties and analysis of active ingredient
• Category 3
  Studies for the determination of mutagenic and carcinogenic properties (in vitro and in vivo)
• Category 4
  Ecotoxicological studies for the determination of the impact on aquatic and terrestric organisms
• Category 5
  Studies for the determination of the behaviour in soil, water and air, bioaccumulation and metabolism studies
• Category 6
  Studies for the determination of residues
• Category 8
  Analytical determinations in biological materials