New EU Clinical Trial Regulations

Explore the challenges and benefits for biotechs conducting trials in the EU, and why partnerships are crucial to support the trial journey, as they discuss:

EU’s complex transition to CTIS
Regulatory and cost differences across EU countries
Patient diversity and recruitment
Ensuring regulatory compliance
Impact of CTR on streamlining processes
EMA vs FDA
Importance of CRO partnerships with local expertise

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Maximizing value across drug development: Embracing a new CDMO and CRO partnership approach

In this webinar, we will present key insights from preliminary findings by the TUFTS Center for the Study of Drug Development, exploring how a comprehensive model that brings CDMO and CRO services under one roof can significantly impact the expected Net Present Value (eNPV) of drug development programs. We will demonstrate how streamlined services across drug substance, drug product, and clinical research can enhance efficiency, reduce timelines, and ultimately deliver high-quality therapies to patients faster. Key takeaways include:

New EU Clinical Trial Regulations

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