Conducting on-site training in all domain (both practical and theoretical). Planning and designing of Vivarium, In-vitro Laboratories.In silico toxicity predictions including risk assessment of potential genotoxic impurities in drug candidates and marketed products.Toxicological assessment of starting material and intermediates.Toxicological evaluation of impurities in final products.Industrial hygiene risk assessment and occupational exposure limit settings.Toxicological support for REACH registration processes, e.g. searches for compilation of available toxicological information, data gap analysis, analysis of read-across possibilities and preliminary categorization.Literature and database searches, tailor-made for specific needs.Working with clients globally for outsourcing of Toxicity/Analytical Chemistry, BA/BE, PK/PD, Exploratory studies.Connecting CROs to clients globally for study outsourcing.

Worked as Study Director Genetic Toxicology.

Responsibilities include to establish In Vitro lab in compliance of GLP. Established in vivo and in vitro genetic toxicity assays. Preparing lab plan right from the construction to instruments installation. Performed acute, sub accute and 28 day repeated dose studies and was responsible for the clinical pathological analysis of biochemical parameters.

Worked as Study Director in genetic toxicology.Performed in vitro and in vivo genetic toxicology studies.