Course Summary
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.
College Link
Career Sectors
This course prepares you for working in the Career Sectors below. Follow the links to get a fuller understanding of the sectors you are preparing for.
Entry Requirements
- The UCD MSc in Toxicology and Regulatory Affairs is designed to accommodate applicants who have successfully completed a four year primary degree programme (minimum of a 2.1 honours or equivalent) in a biological or chemical science. This includes a BSc in Biotechnology, Biochemistry, Microbiology, Genetics, Neuroscience, Physiology, Pharmacology, Toxicology, Medicinal Chemistry or an equivalent qualification.
- An English Language qualification, which includes a minimum score of 6.5 in the International English Language Testing System (IELTS). Other evidence of proficiency in English may be accepted such as the Cambridge Certificate, TOEFL or Pearson’s Test of English.
You may be eligible for Recognition of Prior Learning (RPL), as UCD recognises formal, informal, and/or experiential learning. RPL may be awarded to gain Admission and/or credit exemptions on a programme. Please visit the UCD Registry RPL web page for further information. Any exceptions are also listed on this webpage. https://tinyurl.com/2ae2ffax
Application Details
How to apply?
The following entry routes are available:
MSc Regulatory Affairs and Toxicology FT (F167)
Duration
1 Years
Attend
Full Time
Deadline
Rolling*
MSc Regulatory Affairs and Toxicology PT (F168)
Duration
2 Years
Attend
Part Time
Deadline
Rolling*
* Courses will remain open until such time as all places have been filled, therefore early application is advised
Next Intake: September 2025.
Fees
MSc Regulatory Affairs and Toxicology (F167) Full Time
EU fee per year - € 9300
nonEU fee per year - € 29100
MSc Regulatory Affairs and Toxicology (F168) Part Time
EU fee per year - € 4450
nonEU fee per year - € 14550
***Fees are subject to change.
The Student
Career Interests
This course is typically suited for people with the following Career Interests. If these interests do not describe you, this course may prepare you for work you may not find satisfying.
Investigative
The Investigative person will usually find a particular area of science to be of interest. They are inclined toward intellectual and analytical activities and enjoy observation and theory. They may prefer thought to action, and enjoy the challenge of solving problems with sophiscticated technology. These types prefer mentally stimulating environments and often pay close attention to developments in their chosen field.
Administrative
Administrative people are interested in work that offers security and a sense of being part of a larger process. They may be at their most productive under supervisors who give clear guidelines and while performing routine tasks in a methodical and reliable way.
They tend to enjoy clerical and most forms of office work, where they perform essential administrative duties. They often form the backbone of large and small organisations alike. They may enjoy being in charge of office filing systems, and using computers and other office equipment to keep things running smoothly. They usually like routine work hours and prefer comfortable indoor workplaces.
Career Progression
This focused MSc programme has been developed in consultation with global industry partners and regulatory authorities, and will comprehensively prepare graduates for diverse careers in pharmaceuticals, biopharmaceuticals, medical devices, food, cosmetics, personal care products and chemical sectors. All aspects of product lifecycle management are explored including discovery and invention, quality and CMC, non-clinical testing, management of clinical development, and postmarketing activities. Our graduates are trained in lifecycle and dossier management, regulatory submissions, auditing, pharmacovigilance and safety reporting. They also receive comprehensive instruction in toxicological science, risk assessment and risk management. Graduates will gain the required level of professional ability to operate as independent regulatory toxicologists by developing a sophisticated level of data interpretation, strong communication skills, excellence in problem-solving, and the ability to critically evaluate and form judgements on complex toxicological problems.