Our September 2022 webinar shed light on the recent developments in the EU regulation and its impact on the management of clinical trial supplies.
Two regulatory professionals…
- Frances Smith, Regulatory Compliance Manager, Almac Clinical Services
- Harry Berlanga, Senior Director, Quality, EMEA, Thermo Fisher Scientific
…shared their expertise, touching upon topics such as:
- the new Clinical Trials Regulation
- the European regulatory framework
- the increasing prevalence of virtual audits during the pandemic
- the role of the EU Qualified Person (QP) when an IMP is manufactured in Asia
The slides from the webinar are available here:
Click here for more information about the Asia-Pacific Clinical Supplies Webinar Series
