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This program equips current regulatory affairs professionals in the pharmaceutical sector with comprehensive knowledge of modern diagnostic and medical device regulations while cultivating essential skills for thriving in the fast-paced regulatory environment. Participants will learn to design and execute worldwide strategies for pharmaceutical, biologic, and medical device development and assessment, while applying fundamental and advanced pharmaceutical science principles to drug and biologics research. The Master's program aims to empower graduates to broaden their career prospects and take on expanded roles post-completion. Additionally, it facilitates valuable networking opportunities within the pharmaceutical field through peer interactions during coursework and engagement with industry specialists during dissertation research.
A second-class honours degree in science, engineering, quality, pharmaceutical or regulatory affairs or cognate areas. Those failing to meet the classification requirement may be eligible for entry to the Postgraduate Diploma.
Candidates with significant experience in: pharmaceutical operations, quality engineering, device design, mid to senior management in industry, other professionals who wish to upskill in the regulatory affairs environment, regulatory affairs personnel themselves who want to upskill (as determined by the Institute’s recognition of prior learning policy), in addition to an honours primary degree in another discipline area may also be considered for entry.
English Language Requirements:
IELTS: 6
TOEFL - Computer Based Test: 213
TOEFL - Internet Based Test: 80
TOEFL - Paper Based Test: 575
TIE: C1
TOEIC: 660
Cambridge Exams: FCE (Grade B)
Cambridge Certificate of Proficiency in English; Grade C
Cambridge Certificate in Advanced English: Grade B
CEFR: Low C1
ETAPP: C1
PTE (Academic): 55
QQI FET: Merit
Duolingo English Test : 100
Oxford Test of English: 125 (with a minimum of 100 in each component)
Language Cert: B2 Communicator (with a minimum average of 33)