Roadmap to successful drug therapy partnerships

Join our upcoming webinar with Cara Begg, Alliance Manager and Dr. Katryn Allen, Director of Business Development at Eurofins Clinical Trial Solutions to discover the comprehensive logistics of sample management and analysis across multiple global clinical trial sites. Our speakers will explore the general timelines and necessary steps from initial lab engagement to final data reporting. Plus, gain insights into regulatory assay requirements and the vital role of reagents in ensuring compliance. Participants will also learn about the needs of custom assay development projects, in support of pre-clinical or clinical studies.

Key learning objectives

Gain insights into the requirements and challenges of custom assay development
Discover the benefits of partnering with a central lab for the execution of clinical trials
Explore the workflow and responsibilities from sample logistics to data reporting

Who should attend?

Pharma
Contract research organizations (CROs)
Translational medicine
Director of clinical operations
Bioanalytical scientists
Project managers and project directors
Vendor mangers
Alliance mangers
Medical monitors
Clinical research associates (CRAs)
Clinical Trial Managers (CTMs)
Associate director bioanalysis and Director bioanalysis

Certificate of attendance
All webinar participants can request a certificate of attendance, including a learning outcomes summary, for continuing education purposes.