In the Asia Pacific region specifically regulatory and legal requirements vary from country to country and this is additionally layered by intricate country language requirements.
TORONTO (PRWEB) December 17, 2020
Managing safety cases is becoming more complex due to the ever-increasing volume and variety of data. In the Asia Pacific region specifically regulatory and legal requirements vary from country to country and this is additionally layered by intricate country language requirements. Over the last few years, pharmacovigilance requirements have evolved considerably and more changes are on the horizon.
This webinar will provide an insight into safety regulations in Taiwan, China, and Japan, delving deeper into the recent and upcoming safety regulations in Korea, to support understanding and compliance in pharmacovigilance. It will cover the latest regulatory intelligence, medical writing customisations and explore methods to achieve operational efficiency through system optimization.
Join expert speakers from ICON, Si-Nae Lee, Senior Drug Safety Manager, Safety Reporting; and Mary Pilkington, PhD, Medical Writing Manager, in a live webinar on Tuesday, January 12, 2021 at 4pm CST (China).
For more information, or to register for this event, visit Managing Safety Reporting in the Evolving Regulatory Environment of the Asia-Pacific Region.
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