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 on-demand webinar provides a comprehensive overview of requisition form challenges and solutions, setting the stage for actionable strategies to modernize biospecimen management. Viewers will leave equipped with practical insights to enhance their operations while navigating the evolving regulatory landscape.
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