Fundamentals of Health Products Regulation (Classroom & Asynchronous e-learning)
Training Provider: NATIONAL UNIVERSITY OF SINGAPORE
Course Reference: TGS-2024043273
S$1,620
Original: S$5,400
Save S$3,780
About This Course
This module lays the foundational basis of regulatory management and decision-making for health products, and covers the essential principles in managing pharmaceuticals and medical devices across their life cycles. Regulatory requirements for the different product development phases will be showcased, and hands-on practical sessions will help participants learn about the real-life settings in regulatory decision-making. In this course, participants will also learn about the major regulatory organisations steering the innovation of regulatory processes and focus.
What You'll Learn
Regulation of health products is controlled by standards, guidelines and legal frameworks. The interactions among these and the stakeholders – industry, regulatory authorities, healthcare professionals and patients – are required for effective governance for timely access and safe, quality and efficacious medicines and medical devices for patients.
Entry Requirements
1. Bachelor's Degree.
2. Relevant experience in the field of health products regulatory affairs
Course Details
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