This full-time Master's programme provides a comprehensive overview of drug safety practices within the drug development process. It addresses key aspects of preclinical drug evaluation through the study of: Drug discovery and development Safety pharmacology Mechanisms of drug-induced toxicities Regulatory affairs Bioanalytical sciences It will give you state-of-the-art training in preclinical toxicology, with an emphasis on the molecular in vitro and in vivo aspects of toxicology and safety pharmacology assessments.