Recent Developments in the Global Regulatory Landscape
Postponed from Sep 9 to Sep 30
Adjusting to regulatory changes and global trends are key factors for effectively managing clinical supplies in the EU. Please join us for our upcoming webinar where we will discuss recent developments in the regulation of clinical trial supplies.
Topics include the new Clinical Trials Regulation, the European regulatory framework, the increasing prevalence of virtual audits during the pandemic and the role of the EU Qualified Person (QP) when IMP is manufactured in Asia.
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