Course Summary
This course is aimed at individuals with a scientific qualification who wish to develop their skills and knowledge of regulatory affairs and toxicology, and to gain a recognised third-level qualification in the area. Current, practising toxicologists will also benefit from undertaking individual modules for continuing professional development (CPD), as all of the modules will contribute towards maintenance of professional toxicological accreditation.
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://www.ucd.ie/registry/prospectivestudents/admissions/rpl/
Application Details
Apply online
Who Should Apply?
Full Time option suitable for:
Domestic(EEA) applicants: Yes
International (Non EU) applicants: Yes
Part Time option suitable for:
Domestic(EEA) applicants: Yes
International (Non EEA) applicants: Yes
F167 Regulatory Affairs & Toxicology (Master of Science) Full-Time
Commencing September 2026
Graduate Taught
F168 Regulatory Affairs and Toxicology (Master of Science) Part-Time
Commencing September 2026
Graduate Taught
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.
Duration
2 year part-time (F168).
Delivery: On Campus.
