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This intensive Master's program offers an in-depth exploration of drug safety protocols throughout pharmaceutical development. The curriculum covers essential components of preclinical drug assessment, including: Drug discovery processes, Safety pharmacology principles, Toxicity mechanisms, Regulatory compliance, and Bioanalytical techniques. You'll receive cutting-edge instruction in preclinical toxicology, focusing particularly on molecular-level in vitro and in vivo toxicology evaluations and safety pharmacology testing. The program includes an independent research project that forms the core of your thesis work. Taught at the prestigious Institute of Cancer Therapeutics, this course equips you with industry-relevant expertise for pharmaceutical careers or regulatory roles, while also preparing you for potential PhD research. Toxicology and safety pharmacology form critical foundations for chemical and pharmaceutical sectors, creating strong demand for specialized professionals in this vital field.