DUBLIN–(BUSINESS WIRE)–The “Understanding Pharmacovigilance Regulations in APAC Training Course” conference has been added to ResearchAndMarkets.com’s offering.
Pharmacovigilance regulations in Asia are dynamic and fast-changing
As the Asia-Pacific region becomes increasingly important for pharmaceutical companies, it’s vital to ensure compliance and safety by staying informed of the latest regulatory developments.
This two-day pharmacovigilance webinar has been designed to provide a comprehensive guide to compliance in this geographic region. It will provide an ideal opportunity to keep up-to-date with the latest Good Pharmacovigilance Practices (GVP) and post market PV operations in China, and post-market pharmacovigilance regulations in Singapore, Malaysia, the Philippines, and Australia.
Our panel of experts from this region will provide an overview of Good Pharmacovigilance Practices and discuss pharmacovigilance-related requirements. Gain key takeaways to better understand the new GVP regulations and pharmacovigilance compliance in these countries.
Don’t miss this opportunity to learn from industry leaders and enhance your knowledge of dynamic and fast-changing regulations in Asia, and the growing market in the Asia-Pacific region.
Benefits of Attending
Certifications:
Who Should Attend:
Key Topics Covered
Day 1
Pharmacovigilance in China – GVP Overview
An Overview of China Pharmacovigilance
China GVP 2021 Introduction and Requirements
Best Practices for Compliance with China’s GVP Requirements
Post-Market PV Operation
PV Operation – Individual Case Study Reports (ICSR)
Periodic Safety Update Report (PSUR)/PBRER
Day 2
Pharmacovigilance Regulations in Singapore, Malaysia, Philippines and Australia
Pharmacovigilance Regulations in Malaysia
Pharmacovigilance Regulations in Singapore
Pharmacovigilance Regulations in the Philippines
Pharmacovigilance Regulations in Australia
For more information about this conference visit https://www.researchandmarkets.com/r/jzrt1q
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