Török Magdolna, ERT

Performance of official duties on the basis of the legislation in force in the fields of chemical safety (REACH registration, CLP regulation, biocides), environment and settlement health, production and distribution of cosmetics: checking compliance with legal requirements; control of risk assessments; preparation of the supervision plan, carry out of audits, making of authority decisions, issuing of resolutions of the authority.

- Main responsibilities such as Study Director activities on General and Reproductive/ Developmental Toxicology studies of pharmaceutical and chemical/agro-chemical products - Collaboration with the Sponsor on the study design and prepare a protocol documenting the study details (mainly according to the OECD, US-EPA, ICH guidelines) and direction of the agreed study - Oversight of all scientific and technical activities, monitoring of the in-life phase – to be aware at all times of study status, anticipate problem circumstances that may affect its timing, quality or integrity - Make interim decisions regarding necessary changes, document such changes and agree them with the sponsor as necessary - Review all data to ensure its accuracy and that checking procedures have been observed - Up to date communication with the Sponsor - Data evaluation and report writing in-line with the guidelines listed above and in compliance with international standards. Reports used by the Sponsors in support of marketing authorization and new product approval submissions (including to the European - EMA, ECHA, EFSA-, the US -FDA and EPA- and Japanese - MHLW and MAFF- regulatory authorities) - Scientific representative on internal committees, represent the company at scientific meetings - Train junior scientific and technical staff - Direct/execute research and development strategies consistent with company objectives in GLP environment