Endpoints or to clarify toxicity mechanisms, our in vitro assays contribute to more accurately capturing the safety profile of your test compound, while reducing the use of laboratory animals. Our in vitro toxicity assay portfolio includes assays for GLP regulatory requirements or non-GLP testing, such as screening assays. The latter allows high-throughput in vitro toxicity testing while using only a minimal amount of substance. All assay designs can be tailored to your needs.
In vitro skin irritation: Reconstructed human epidermis (RhE) test method
In vitro skin corrosion: RhE test method
In vitro 3T3 NRU phototoxicity test, according to ICH S10
Skin sensitization assays covering the skin sensitization AOP:
In chemico skin sensitization: Assays addressing the adverse outcome pathway key event on covalent binding to proteins—the direct peptide reactivity assay (DPRA)
In vitro skin sensitization: ARE-Nrf2 luciferase test method
In vitro skin sensitization assays addressing the key event on activation of dendritic cells on the adverse outcome pathway for skin sensitization
Cardiac Safety (According to ICH S7SB Guidelines):
Ion channel screenings (hERG, NaV1.5, CaV1.2) using automated patch clamp robots
Manual ion channel (hERG, NaV1.5, CaV1.2) screenings at normal or elevated temperature
Service Assets
Automated flow cytometry
High-throughput pipetting robots
Camera-based Ames assay unit
Comet imaging station
Fast screening assay variants that require only a minimal amount of substance, for the above-mentioned in vitro tests
QSAR analyses for a first toxicity screening
Tailor-made in vitro toxicity assay development and validation
Expert consultancy services on study design and compound de-risking