Lutfiya Miller, Ph.D., DABT, Scientific Consultant 1, Toxicology
Dr. Lutfiya Miller is a board-certified toxicologist with over a decade of experience in the drug development industry. Dr. Miller began her career as a Study Director for GLP-compliant developmental and reproductive toxicology (DART) studies, where she was responsible for overseeing the design, analysis, interpretation, and reporting of these critical safety investigations.
At Intertek, Dr. Miller leverages her experience in a regulated environment to the conduct of on-site study monitoring for clients’ studies at nonclinical Contract Research Organizations (CROs) worldwide. She ensures that these studies are executed in full compliance with regulatory requirements and uphold the highest standards of scientific rigor.
Dr. Miller's expertise extends beyond the laboratory as she provides advice and guidance to clients in their drug development programs. In this area, she contributes to strategic design of toxicology programs, undertakes the management of toxicology studies, including review of study protocols and reports, and prepares and reviews regulatory submission documents that are critical for obtaining regulatory approvals.
Dr. Miller has published 15 peer-reviewed journal articles, 3 book chapters, and over 30 abstracts that collectively have over 170 citations. She has presented research at 17 conferences across North America and Japan and has won 14 research-related awards. She has also lectured in several undergraduate courses relating to embryonic development and developmental toxicity, and supervised undergraduate research projects.
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