"Over 10 years of experience within preclinical development at LEO Pharma. Preclinical writing and project planning within several stages of drug development, registration of the new drug and post-marketing activities. 14 years of experience from Danish Toxicology Centre (DTC): Nonclinical safety and risk assessments of the drugs and related substances (expert reports). Regulatory toxicology experience with pharmaceuticals and other chemicals (industrial chemicals, biocides etc.) and biologicals. Health and safety assessment of chemical compounds, development of quality criteria for soil, water and air. --------- 1996-2005: For the purpose of notification of new chemical substances in the European Union, project planning, test programme monitoring, notification and risk assessment of new chemical substances. 1993-97: Safety assessment of over 10 chemicals for the purpose of harmonised labelling and classification in Norway, Sweden and the EEC. 1999: Environmental and health hazard assessment of brominated flame-retardants for the Danish Environmental Protection Agency. About 12 compounds were selected based on results from a Danish mapping/mass flow project. 1992-93: Project leader for the toxicological testing of ergot infested grass seeds in lambs. The practical work took place at Tjøtta Forskingsstasjon, The Norwegian State Agricultural Research Stations, Norway, in collaboration with Department of Large Animal Clinical Sciences, Norwegian College of Veterinary Medicine. 1990-96: Toxicological safety assessment of about 15 pesticides based on documentation submitted for Danish registration purpose. The work was performed in a period from 1990 to 1996 for the Danish Environmental Protection Agency, and the assessment reports were used in the governmental decision process. Specialties: Special experience in toxicological database searching"  

Toxicology, Drug Development, Pharmaceutical Industry