Toxicologic Pathology and Environmental Testing

As global concerns rise regarding environmental exposures and their health effects, toxicologic pathology is gaining renewed attention. This session focuses on the pathological evaluation of tissue changes resulting from exposure to chemical, pharmaceutical, and environmental agents. Attendees will delve into the assessment of organ toxicity, dose-response relationships, and the mechanisms underlying toxic injuries. Presentations will include case studies in preclinical drug testing, industrial toxicology, and environmental risk assessments. Emphasis will be placed on integrating histopathological findings with biochemical and molecular data to predict potential human toxicity. The role of Good Laboratory Practice (GLP) standards, regulatory frameworks, and international safety guidelines will be discussed in detail. This session will also highlight the importance of nonclinical safety assessments in the drug development pipeline. Participants will gain a deeper understanding of how toxicologic pathology contributes to public health protection, regulatory compliance, and the safe introduction of new chemicals and therapies into the market.

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