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Objectives

This course will provide students an appreciation of current scientific and regulatory guidance for the optimization and control of pharmaceutical manufacturing processes for the quality assurance purposes. Students will learn about the optimal operation of pharmaceutical manufacturing processes via the array of carefully curated topics in this course, including the theory and principles of process optimization and control, as well as the regulatory framework for quality assurance. With a focus on real-world applications and case studies, students will learn to navigate the complexities of pharmaceutical manufacturing, ensuring compliance and control at every step.

Who Should Attend

E.g. Process development/MS&T engineer, QA specialist, QC laboratory analyst/chemist, production executive/engineer/biotechnologist, regulatory specialist, regulatory professional/lead/executive, product application specialist, formulator, research scientist/associate/assistant

Entry Requirements

One of the following degrees, or their equivalent:

Bachelor of Science in Chemistry, OR;• Bachelor of Science in Life Sciences, OR;• Bachelor of Applied Science in Food Science & Technology, OR;• Bachelor of Applied Science in Applied Chemistry (Drug Option), OR;• Bachelor of Science in Pharmacy, OR;• Bachelor of Engineering (Chemical Engineering)

Class Schedule

Wednesday (6.00 PM - 8.00 PM)

Tutorial Schedule

Same day as Lecture

Lesson Delivery

a) Lecture - 2 hours b) Tutorial - 0 hours c) Project - 6 hours d) Preparation - 2 hours

Full Fees (before GST)

S$5400.00

Nett Fees payable after SSG Funding

Please note that the mode of delivery is subject to change in light of the COVID-19 situation. Courses marked ‘online’ may have compulsory face-to-face sessions such as laboratory or hands-on components and details should be sought from the schools or departments before learners register for them.