- SMIMA1081U - Drug Regulatory Affairs in Drug Development
- SMIMA1091U - Quality by Design (QbD) in Pharmaceutical Development
- SMIMA1161U - Drug Formulation and Delivery
- SMIMB1011U - Discovery and Development of Medicines
- SMIMB1041U - Pharmacology
- SMIMIF115U - Market Access for Pharmaceutical Products – trends and challenges
- SMIMIL014E - Master's project
- SMIMIL02IE - Independent Elective Study
- SMIMIL171U - Biopharmaceuticals Drug Development
- SMIMIL172U - Deal-making in the Pharmaceutical Industry
- SMIMM1141U - Chemical Process Development and Production of Active Pharmaceutical Ingredients (API)
- SMPMA0014E - Master's project
- SMPMA3141U - Regulatory Affairs in the EU
- SMPMA3151U - Regulatory Strategic Considerations during Global Drug Development
- SMPMA3161U - Quality - Drug Substance and Drug Product
- SMPMA3171U - Non-clinical Documentation
- SMPMA3181U - Clinical Development and Documentation
- SMPMA3191U - Product Life Cycle Activities
- SMPMA3201U - Role and Responsibilities of a Regulatory Affairs Professional
- SMPMA3211U - The Regulatory Affairs Environment in the USA
- SMRMIF000E - Exam in Regulatory Affairs in the EU
- SMRMIF000U - Course in Regulatory Affairs in the EU
- SMRMIF001E - Exam in Regulatory Affairs in the USA
- SMRMIF001U - Course in Regulatory Affairs in the USA
- SMRMIF002U - Ethical, societal and assessment aspects of the regulation of medicines
- SMRMIF003E - Exam in Clinical Development – Efficacy of Medicines
- SMRMIF003U - Course in Clinical Development – Efficacy of Medicines
- SMRMIF005U - Safety of Medicines - from Non-clinical Development to Pharmacovigilance
- SMRMIF006E - Exam in Quality – Active Substance and Medicinal Product
- SMRMIF006U - Course in Quality – Active Substance and Medicinal Product
- SMRMIF007E - Exam in Biopharmaceuticals – Quality Development and Documentation
- SMRMIF007U - Course in Biopharmaceuticals – Quality Development and Documentation
- SMRMIFI01U - Independent Elective Study
- SMRMIFS01U - Master's project