这个全日制硕士课程提供了药物开发过程中药物安全实践的全面概述。它通过研究药物发现和开发，安全药理学，药物诱导的毒性机制，法规事务，生物分析科学来解决临床前药物评估的关键方面。它将为您提供临床前毒理学方面的最新培训，重点是毒理学和安全药理学评估的体外和体内分子研究。作为该计划的一部分，您将进行一个原创的研究项目，这将是您论文的基础。
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 and 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. As part of the programme you will undertake an original research project that will be the basis of your dissertation. Delivered at the Institute of Cancer Therapeutics, an internationally renowned research institution, the programme gives you the skills you need for a career in the pharmaceutical industry or regulatory bodies, along with the foundations for PhD study. Drug toxicology and safety pharmacology lies at the heart of the chemical and pharmaceutical industries, and demand for highly skilled practitioners in this field is extremely high.