Dr. Kimberly Ehman has over 20 years of toxicology and medical device experience. As director of Regulatory Toxicology, she offers expertise in toxicological risk assessments for medical devices, food and beverage products, and electronic nicotine delivery systems. Dr. Ehman previously worked as a toxicologist for RTI International, Toxicology Regulatory Services, and Altria Client Services. In her current position, Dr. Ehman provides technical and regulatory support for biocompatibility test programs and conducts quantitative toxicological risk assessments to support product safety and risk management decisions.