Two Key Guidelines for the Assessment of Skin Irritation: OECD TG 404 and ISO 10993-23:2021In the biocompatibility assessment of c...
Toxicology Studies
Comprehensive Toxicology Testing for Regulatory Safety Assessment
Toxicology studies are a cornerstone of non-clinical safety evaluation, providing critical data on the potential adverse effects of substances on biological systems. These studies are essential for regulatory submissions, product development, and risk assessment across pharmaceuticals, medical devices, cosmetics, biocidal products, and chemical substances.
Our laboratory conducts toxicology studies under robust quality systems aligned with OECD Good Laboratory Practice (GLP) principles when required, ensuring that all generated data is scientifically reliable, traceable, and internationally accepted.
Integrated Regulatory Approach
Genotoxicity studies are often used as part of a broader toxicological safety assessment strategy. Results are interpreted in combination with other toxicity endpoints to provide a complete safety profile for regulatory submissions.
When performed under GLP conditions, all experimental steps are fully documented, independently reviewed, and archived to ensure transparency and reproducibility.
From Repeated-Dose Toxicity to Carcinogenicity: Long-Term Safety Assessment Using OECD Test Guidelines 407, 408, 452, and 453Under...
OECD Guidelines for Acute Inhalation Toxicity: The Right Testing Strategy Using TG 403, TG 433, and TG 436The respiratory tract is...