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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:
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
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2:2 or above in a related scientific discipline e.g. Biosciences, Chemistry, Biomedical, Medical, Pharmaceutical, Pharmacological, or Toxicological Sciences. Applications are also welcome from candidates with non-standard qualifications, who have significant relevant experience; each case will be considered on its merits.
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