Regulatory Affairs & Toxicology
Toxicology is the study of how man-made and naturally occurring substances can have adverse effects on humans, animals, plants, and the environment, and how these effects can be minimised or avoided. Regulatory Affairs is a closely related field that focuses on applying toxicology for the protection of public health in the areas of human medicines, medical devices, biotechnologies, foods, agrichemicals and cosmetics. These courses explore the important role of toxicology in modern society with particular focus on the pharmaceutical, food and chemical industries.
The UCD MSc Regulatory Affairs & Toxicology provides the theoretical and practical knowledge needed to understand the latest toxicological techniques and the current regulatory landscape.
- This course has been specifically developed to prepare graduates for careers in highly regulated industries including pharmaceuticals and biopharmaceuticals, medical devices, foods, personal care products and chemicals
- The course is run by European Registered Toxicologists (ERT), with expert guest lecturers from industry, and national and international regulatory bodies
- The course is approved for accreditation toward becoming a registered toxicologist and for CPD credits toward maintaining registered toxicologist accreditation.
- Internships are available with industry partners, regulatory authorities and toxicology consultancy companies