Roadmap To Successful Drug Therapy Partnerships

This session details the comprehensive logistics of sample management and analysis across global clinical trial sites. Cara Begg, Alliance Manager, and Dr. Katryn Allen, Director of Business Development, outline general timelines and necessary steps, spanning initial lab engagement through final data reporting. They also cover regulatory assay requirements, the critical role of reagents in ensuring compliance, and the specific needs of custom assay development projects supporting pre-clinical or clinical studies.

Key Learning Objectives:

• Review requirements and challenges in custom assay development.
• Identify the benefits of leveraging a central lab for clinical trial execution.
• Understand the full workflow and responsibilities, from sample logistics to data reporting.