Lauren NAKAB

Planification, organization and managment of Genetic Toxicology Studies: manager for the general conduct of the studies in accordance with the Good Laboratory Practices
Perfect commend of the reglementary genotoxic tests (Ames test, MLA/TK, Chromosomic aberration test, Micronucleus test, Comet Assay, UDS) and of some other in vitro studies (Phototoxicity 3T3NRU, Irritation and Corrosion on RHE).
Close collaboration with the Quality Assurance Unit and with the laboratory technician.
Scientific, technical and commercial contact with Sponsors and Test Sites for multisite studies.
Close involvement to the general organisation of the laboratory (informatical validation of the software used in GLP studies, SOP writing...).
Development of new methods of toxicity or genotoxicity evaluation
involvement in the research project of the laboratory and manager for the genotoxicity part of an ANR program.

Protocol writing, carrying out of tests and report writing of studies for sensitization evaluation.

Elaboration of the demand of Pharmaceutical Etablishment

Evaluation of biomonitoring study data and elaboration of a report as part of the european registering of a phytosanitary compound.