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Regulatory Affairs and Toxicology

Graduate Taught (level 9 NFQ, credits 90)

The UCD MSc in Regulatory Affairs and 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 towards becoming a registered toxicologist and for CPD credits towards maintaining registered toxicologist accreditation.
-Internships are available with industry partners, regulatory authorities and toxicology consultancy companies

Toxicology and careers in toxicology are undergoing rapid and dramatic changes as new technologies, new regulations and new discoveries occur at an accelerated rate. The MSc in Toxicology and Regulatory Affairs is aimed at individuals with a scientific qualification who wish to develop their skills and knowledge of toxicology and global regulatory affairs, whilst gaining a recognised third-level qualification in the area. The programme was developed in consultation with international regulatory bodies in the pharmaceutical, biotechnology, food and medical device sectors, and has been designed to provide graduates with industrially relevant expertise in toxicology and regulatory affairs. We aim to produce highly motivated, independent thinkers with well-developed problem-solving ability, who are capable of working effectively in a professional environment either alone or in teams. Successful completion of the MSc and experience working in this area will also allow graduates to apply for registration with the Irish Register of Toxicologists (RTI) which is the national accrediting body for registered toxicologists in Ireland. Accreditation at national level also awards the status of European Registered Toxicologist (ERT), which is required for professional toxicological practice. Current practising toxicologists will also benefit from undertaking individual modules for continuing professional development (CPD), as all of the modules have been developed to contribute towards maintenance of professional toxicological accreditation. The programme includes presentations and lectures from experts in toxicology and regulatory affairs, including external practitioners, giving students the opportunity to learn from leaders in the field. Multiple teaching approaches from our dedicated, expert academic staff facilitate student development throughout this programme. A variety of assessment strategies are also employed, including classical written examinations, presentations and case studies. The programme is offered as a part-time 24 month MSc (F110) or a full-time 12 month programme (F130). There is also the option to obtain a Professional Certificate, Professional Diploma or Graduate Diploma if students complete sufficient taught modules.

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.

Duration

1 Years full-time / 2 Years part-time

Number of credits

90

Careers or further progression

Graduates of this programme will find employment in toxicological testing and product quality testing within industry or government agencies or in the field of regulatory toxicology within governmental and international regulatory bodies. Graduates may also enrol in PhD programmes and further academic studies in related disciplines.

Further enquiries

Contact Name: Craig Slattery
email: biotech@ucd.ie

Subjects taught

This is a full-time, one-year programme, divided into three semesters (from early September until the end of August). The programme consists of lectures, tutorials, seminars, workshops and case studies. To complete the MSc in Regulatory Affairs and Toxicology, you must successfully complete 8 core modules. You must also successfully complete a research project which includes an internship placement with a regulatory authority or a relevant industrial partner.

Comment

Approved for accreditation towards becoming a registered toxicologist and for CPD credits towards maintaining IRT/ERT accreditation.

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.

Application date

Deadline - Rolling
* Courses will remain open until such time as all places have been filled, therefore early application is advised

Course fee

MSc Regulatory Affairs and Toxicology (F167) Full Time
EU fee per year - € 7530
nonEU fee per year - € 24800

MSc Regulatory Affairs and Toxicology (F168) Part Time
EU fee per year - € 3760
nonEU fee per year - € 12400

***Fees are subject to change

Enrolment and start dates

Next Intake:2019/2020 September

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