Key Accesses to Multinational Clinical Studies Success: Optimized Clinical Supply Management and EU Qualified Person ReleaseProcess

Featured Speaker:

JULIE DELANEY

Site Director,
Catalent Singapore

Julie is an experienced clinical supply professional with 25 years of industry experience, 15 of which have been in the APAC region. She has worked in key clinical supply and quality positions in CDMOs and across the pharmaceutical and bio pharma industry.

Topic: Proactive Strategies to Evaluate and Mitigate Clinical Supply Risk

Abstract for presentation:

This session focuses on strategies that build an understanding of risk assessment within clinical supply planning, as well as how studies’ protocol requirements, drug characteristics, packaging specifications, and patient compliance concerns must be identified and addressed in order to mitigate risk to help achieve successful clinical supply outcomes. Julie will also discuss packaging and clinical supply chain services for global clinical trials with a specific focus on APAC region.

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