Dr. Tanja Wildemann

Hazard assessment, risk assessment

- Preparation of safety assessments for cosmetic ingredients (chemically defined substances and plant extracts), fragrances according to EU Cosmetics Regulation EC/1223/2009 and Notes of Guidance - Read-across and in silico methods: OECD QSAR toolbox, DEREK, Toxtree - Study monitoring - Provision of toxicological advice to customers and other departments (e.g. R&D, Business Units, production) - Regulatory support with regard to e.g. cosmetic regulation - Representative in trade association meetings

- Preparation of electronic dossiers for plant protection products (Regulation (EC) 1907/2006), chemicals (Regulation (EC) 1107/2009), biocides for registration and re-registration; - Classification of chemicals (Regulation (EC) 1272/2009) based on available toxicological data - Study monitoring - Human health risk assessments - IUCLID, OECD QSAR toolbox

Management of the task forces on Novel Foods and Nanotechnology, Packaging Materials, Risk Assessment of Genotoxic Carcinogens and Threshold of Toxicological Concern (TTC): - the organisation of meetings, including the agenda, annexes and minutes, - supporting the research of international experts and the publication of scientific articles, - the organisation of workshops, symposia (up to 350 participants), - budget preparation, - ensuring close working relationships with EC, EFSA, WHO, US FDA.

Food safety, information management and technology, project management, web design

Cardiovascular toxicology, human health risk assessment