We provide clients in the chemical industries with toxicology and product safety assessment guidance during safety testing phase. We work with clients in the evaluation and interpretation of the safety of existing and potential products, metabolites, degradants impurities and intermediates. We review licensed candidates and perform due diligence audits as well.

We design study specific protocols, initiate, monitor and report GLP and screening preclinical studies. We can also place studies with a reliable worldwide network of contract research organizations. Vast experience is utilized in monitoring preclinical animal studies, including general toxicology (acute to repeated dose), carcinogenicity, reproductive toxicology, teratology, in vitro and in vivo genetic toxicology and safety pharmacology. Services are also available for auditing and reviewing studies conducted internally or at outside laboratories. We prepare all toxicology components for regulatory submissions.

• Toxicology program design
• Clinical Research Organization (CRO) selection
• Contract management
• Project management
• Study protocol development and review
• Study monitoring on behalf of clients
• Report review and expert opinions
• Dossier for regulatory submission