Effective JAPAC Safety Strategies and Regulatory Considerations

Available on-demand

On-demand webinar

Join local safety and regulatory experts for fresh insights that will explore the ongoing changes in JAPAC and reveal key strategies for managing them.

Register now to learn valuable information about:

Navigating the evolving local safety and regulatory guidelines for JAPAC
How the recent adoption of Good Pharmacovigilance Practices (GVP) has impacted China
Increasing efficiencies across JAPAC with Robotic Process Automation (RPA)
Mastering the pharmaceutical nuances and reporting requirements in Japan
Taking advantage of IQVIA’s expertise in local case processing for Japanese language, Chinese database efficiency, and local safety and regulatory services across JAPAC

Meet the Speakers

Hye Jin Choi, R. Ph

Senior Director, Regulatory Affairs & Drug Development Solutions (RADDS),

IQVIA Asia Pacific

Dr. Jayawant Fuke

Senior Director, Lifecycle Safety,

IQVIA

Register now to watch on-demand!

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