Abstract

This article examines the critical role of integrating toxicology in approval processes within the regulatory landscape. As regulatory agencies worldwide strive to ensure consumer safety and environmental protection, the incorporation of toxicology studies becomes pivotal in evaluating potential risks associated with various products. This integration not only safeguards public health by assessing the adverse effects of chemicals, drugs, and agents on living organisms, but also enhances industry standards by promoting research and development for safer and more reliable products. The challenges and advances in toxicology integration are explored, highlighting the collaborative efforts between regulatory bodies, researchers, and industries to establish guidelines and frameworks for toxicity testing. Ultimately, the article underscores the essential balance between innovation and safety through the seamless integration of toxicology in regulatory approval processes.