Justine practices in the areas of life sciences, health, and regulatory compliance. She advises manufacturers throughout the lifecycle of pharmaceutical products and medical technologies. From product design through to commercialization, she supports companies on matters relating to compliance, regulatory responsibilities, and interactions with health authorities.
With a background in law and a master’s degree in biology, Justine has a deep understanding of the scientific, technological, and legal issues that shape the industry. Her interdisciplinary training enables her to provide practical, tailored advice in complex and constantly evolving regulatory environments.
Justine is also interested in emerging issues in clinical research. She has published an essay analyzing the normative obligations of physician researchers in clinical trials involving human cerebral implants. Her work examines the legal, ethical, and scientific dimensions of prematurely terminated studies and their impact on participants, while proposing potential solutions grounded in the Quebec and Canadian regulatory frameworks.
