Master's
MSc Regulatory Affairs & Toxicology – UCD
Course Overview
The MSc Regulatory Affairs & Toxicology provides advanced knowledge of the processes involved in evaluating the safety, effectiveness, and compliance of healthcare and pharmaceutical products. Students study toxicological assessment, regulatory frameworks, drug safety, risk management, clinical trials, pharmaceutical regulations, and quality systems through applied learning.
The programme develops expertise in interpreting scientific data and managing regulatory requirements across healthcare industries. Students gain skills required to support safe product development and regulatory approval processes. Graduates are prepared for careers in pharmaceutical companies, regulatory agencies, biotechnology industries, quality assurance, and healthcare compliance.
Entry Requirements
- Completion of 10 + 2 (Higher Secondary Certificate) with a minimum aggregate of 75%–80% including Chemistry and Mathematics.
- IELTS 6.5 (with no band lower than 6.0), TOEFL iBT 90, PTE 63, or Duolingo 120.
- Chemistry background review and laboratory safety check.
- Certified 10 + 2 mark sheets, official transcripts, statement of purpose, and academic recommendation letters.
- Valid passport copy, visa eligibility verification, and academic credential assessment.
Career Outcomes
- Regulatory Affairs Specialist
- Toxicology Associate
- Pharmaceutical Compliance Officer
- Safety Assessment Scientist
- Regulatory Consultant
Scholarship Available
- Yes (UCD Postgraduate Scholarships)
