A decade ago, Duke-NUS Medical School established the Centre of Regulatory Excellence (CoRE) to enhance health products regulatory systems and competency across ASEAN and the broader Asia-Pacific region. CoRE is pivotal in supporting policy innovation and facilitating progress towards effective and efficient health products regulation. As a neutral academic platform, CoRE bridges the gap between industry and regulators, fostering the development of future regional regulatory leaders for the healthcare ecosystem.
In line with its mission, CoRE offers a series of onsite training courses in Singapore, providing participants with practical insights, including two Graduate Certificate programmes that cover topics across pharmaceuticals, advanced therapies and medical technology e.g.
- Fundamentals of Health Products Regulation
- Regulation of Pharmaceutical Manufacturing
- Manufacturing and Quality Management Systems for Medical Devices
SeerPharma has been invited to contribute to CoRE's upcoming course on the Fundamentals of Health Products Regulation, scheduled from September 9th to 13th, 2024.
At this workshop, SeerPharma will lead sessions on key concepts in Good Manufacturing Practices (GMP), including:
- Failures in GMP
- History of GMP
- Basic GMP requirements, including definitions and quality management
Additionally, SeerPharma will provide an overview of GMP compliance, audits, and inspections, drawing on over 35 years of experience in addressing industry challenges related to Quality and GMP.
We are honoured to support this session and contribute to the ongoing mission and efforts of Duke-NUS CoRE.
For more information on this upcoming workshop, please visit: https://www.duke-nus.edu.sg/core/events/upcoming-events/detail/index/2024-gms5003-fundamentals-of-health-products-regulation
Initiatives such as this, re-affirm our commitment to “Advancing Quality and GMP Best Practices in the APAC region”.