What Regulatory Guidelines Govern Toxicology in the Pharmaceutical Industry?
Several regulatory guidelines govern toxicological assessments in the pharmaceutical industry. The most prominent ones include guidelines from the Food and Drug Administration (FDA) in the United States, the European Medicines Agency (EMA) in Europe, and the International Council for Harmonisation of Technical Requirements for Pharmaceuticals for Human Use (ICH). These guidelines outline the required toxicology studies and the standards for conducting them.
