Post-Market Activities for Pharmaceuticals (Classroom & Asynchronous e-learning)
Training Provider: NATIONAL UNIVERSITY OF SINGAPORE
Course Reference: TGS-2024044123
S$1,620
Original: S$5,400
Save S$3,780
About This Course
This course will allow participants to understand the damaging implications of poor quality medicines to public health, as well as the evolving challenges in minimising the entry of these substandard medicines and falsified products. Participants will learn the regulatory controls along the entire distribution and supply chain of medicines, and the good practices and standards expected. Through practical exercise, participants can gain practical insights on the assessment of quality defects and detection of falsified medicines.
What You'll Learn
The assurance of safe and quality medicines in the market depends on a range of vital activities after the approval of a medicine by the authorities. This includes the continual monitoring offered by inspections and audits of facilities and testing of product quality. In this globalised environment, there is also an increasing need to leverage on networks to effectively detect lapses in product quality and services in a timely manner.
Entry Requirements
1. Bachelor's Degree.
2. Relevant experience in the field of health products regulatory affairs
Course Details
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