What Role Do Toxicology Standards Play in Pharmaceuticals?
In the pharmaceutical industry, toxicology standards are critical for drug development and approval. They guide the design of preclinical studies to evaluate the safety profile of new drug candidates. Regulatory agencies such as the Food and Drug Administration (FDA) require extensive toxicological data before granting approval for human clinical trials. These standards ensure that any potential risks are identified and mitigated early in the drug development process.
