Description
Regulatory Violence presents a critical analysis of how regulatory systems function in biomedicine and health globally. Margaret Sleeboom-faulkner investigates the concept of regulatory violence—the structural and systemic impacts of regulatory frameworks on biomedical research, drug development, and healthcare delivery.
The book explores regulatory experimentation across different countries and regions, examining how regulatory decisions and policies affect scientific innovation, patient access to treatments, and public health outcomes. Through case studies and comparative analysis, Sleeboom-faulkner demonstrates the complex interactions between regulatory bodies, pharmaceutical companies, researchers, and patients.
Drawing on bioethics and law perspectives, this work reveals tensions between protecting public safety, advancing medical innovation, and ensuring equitable access to healthcare. It contributes to understanding how regulatory frameworks can both enable and constrain biomedicine globally.
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