The Future of Requisition Forms

As clinical trials become increasingly complex, and as ICH E6(R3) calls for more robust regulation of the systems and processes that dictate biospecimen operations, the need for efficient, accurate, and connected requisition form workflows has never been more critical. This webinar will provide a comprehensive overview of requisition form challenges and solutions, setting the stage for actionable strategies to modernize biospecimen management. Participants will leave equipped with practical insights to enhance their operations while navigating the evolving regulatory landscape. Don’t miss this opportunity to hear directly from industry experts about how your organization can stay ahead of the curve in biospecimen management while meeting ICH compliance requirements.

Attendees will gain insights into:

• Paper requisition forms vs. lab specific e-requisitions from both sponsor and site perspectives.
• Emerging challenges in biospecimen lifecycle management, including how ICH E6(R3) compliance reshapes requisition workflows, mandating a move toward digital solutions.
• Innovative strategies to optimize sample tracking and metadata management while addressing site-specific concerns.