Say hello to Emma Pedersen!
New director for Biological Evaluations & Toxicology at Key2Compliance®. Emma Pedersen comes from 11 years at RISE (Research Institutes of Sweden) working as a research scientist, mainly with biological evaluation of medical devices according to ISO 10993 (including in vitro testing under GLP) and replacement of animal testing methods for regulatory purposes.
Emma has been involved in several international development and validation studies regarding in vitro test methods for, e.g., identifying endocrine disruptors. She is a member of the Swedish standardization committee (SIS TK 340) responding to ISO TC194, and has represented Sweden in OECD expert groups on good in vitro method practices (GIVIMP) and validation of non-animal testing methods. She has a broad knowledge regarding medical devices and the corresponding regulatory framework as well as an extensive experience in interdisciplinary work and research.
