Christine M. Palermo, Ph.D., DABT
Director of Regulatory Sciences
T: 202-557-3830
F: 202-557-3836
Overview
Christine M. Palermo, Ph.D., DABT, is Director of Regulatory Sciences at The Acta Group (Acta®). Dr. Palermo provides Acta clients with global strategy in chemical regulatory compliance, risk assessment, and product stewardship, assisting clients to commercialize new products and expand markets for existing product portfolios. Dr. Palermo deploys the extensive U.S. domestic and international experience she gained as a regulatory sciences principal and leader of global toxicology for ExxonMobil (EM) Biomedical Sciences to advise Acta clients regarding ongoing and anticipated regulatory risk management in the United States, European Union (EU), and Asia for new and existing chemicals and chemical products, including those subject to heavy regulatory scrutiny.
Dr. Palermo is a recognized leader in the advancement of science-based regulatory decision-making. Through her involvement with the European Chemical Industry Council (CEFIC), the European Centre for Ecotoxicology and Toxicology of Chemicals (ECETOC), the World Health Organization/International Programme on Chemical Safety Mode of Action/Human Relevance Framework (WHO/IPCS MOA HRF), and other industry organizations, Dr. Palermo has worked to evolve the internationally recognized evidence integration framework for assessing human relevance of chemical mediated outcomes in animals, and to advance technical approaches for endocrine disruptor identification, reproductive hazard identification, and a risk-based polymer safety decision framework to inform chemical management approaches. She has a long and distinguished bibliography of peer-reviewed scientific papers and articles published in Reproductive Toxicology, Toxicology Letters, and Regulatory Toxicology and Pharmacology, among other prominent scientific journals.
Representative Engagements
- Advised a global technology and manufacturing company on international chemical compliance requirements, including substance registration strategies, classification and labeling, supply chain communication, and approaches to addressing differing regulatory requirements across jurisdictions.
- Advised a global distributor in assessing the scope and applicability of EU chemicals and product legislation, including the scope and applicability of Restriction of Hazardous Substances (RoHS) substance restrictions and Conformité Européenne (CE) marking and conformity assessment requirements for products placed on the EU market.
- Assisted a U.S.-based chemicals supplier in EU Registration, Evaluation, Authorisation and Restriction of Chemicals (REACH) and comparable chemical regulatory data-compensation matters, including valuation of regulatory data, negotiation of data sharing arrangements, and preparation and negation of Letters of Access (LoA) and related agreements.
- Managed EU REACH, South Korea Act on the Registration and Evaluation of Chemicals (K-REACH), and Turkey Kimyasalların Kaydı, Değerlendirilmesi, İzni ve Kısıtlanması (KKDIK) obligations for a global chemical supplier through Only Representative (OR) arrangements, including assessment of registration requirements, submission of registration dossiers, management of ongoing compliance obligations, and engagement with supply chain stakeholders.
Professional and Community Involvement
- Diplomate, American Board of Toxicology (ABT) 2010 –
- Member of the Society of Toxicology (SOT) 2001 –
Articles and Writings
Lea IA, Buerger AN, Feifarek D, Mihalchik A, Heintz MM, Haws LC, Nyambego H, Goyak K, Palermo C, Borghoff SJ. 2024. Evaluation of the endocrine disrupting potential of di-isononyl phthalate.
Lea IA, Feifarek D, Mihalchik A, Heintz M, Haws L, Nyambego H, Goyak K, Palermo C, Borghoff SJ. 2024. Evaluation of the endocrine disrupting potential of di-isodecyl phthalate.
Rogers JM, Buerger AN, Palermo C, Heintz MM, Haws LC, Lea IA. 2024. Evaluation of a Sertoli cell based adverse outcome pathway for effects of DINP on the developing male reproductive tract.
Palermo CM, Foreman JE, Wikoff DS, Lea I. 2021. Development of a putative adverse outcome pathway network for male rat reproductive tract abnormalities with specific considerations for the androgen sensitive window of development. Curr Res Toxicol. 2:254-271. doi: 10.1016/j.crtox.2021.07.002.
