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About This Webinar

Sponsored by Slope

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

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When: Tuesday, June 17, 2025 · 11:00 a.m. · Eastern Time (US & Canada)
Duration: 1 hour
Language: English
Who can attend? Everyone
Webinar ID: a3bf7fee5f2e
Dial-in available? (listen only): No
Featured Presenters
Webinar hosting presenter
Vice President, Product, Slope
Brian Smith is Vice President of Product at Slope, where he leads teams focused on Product Management, Biospecimen Data & Operations, and Client Strategy & Success — driving innovation and operational excellence for Slope’s Biospecimen360™ platform. Previously, he held senior leadership roles at Science 37 and ERT, where he spearheaded significant organizational growth, platform enhancements, and strategic partnerships. Brian holds a Bachelor of Science in Biotechnology from the Rochester Institute of Technology.
Webinar hosting presenter
Former Associate Director, Clinical Biosample and Supply Operations, Intellia Therapeutics
Based in Durham, NC, Jarrett Glass is a seasoned clinical biosample operations and management professional. His ten years in clinical research, primarily supporting small- to midsize biotech companies in immuno-oncology and rare disease, have instilled in him the critical importance of agile and compliant sample management. Originating from a commercial cytogenetics laboratory, Jarrett is particularly attuned to the need for meticulous data integrity and the safeguarding of participant rights, principles underscored by upcoming regulatory shifts like ICH E6(R3).
Webinar hosting presenter
Manager, Clinical Research Laboratory - Clinical Trials Office, University of Arizona Cancer Center
Carolyn Lane is a Clinical Research Laboratory Manager with over 10 years of clinical laboratory and pathology experience. She has a strong interest in advancing cancer treatment through clinical trials. Outside of work, Carolyn enjoys spending time hiking, skiing, and traveling with her family.
Webinar hosting presenter
Senior Clinical Research Laboratory Manager, UPMC Hillman Cancer Center
Jamie Voyten is a Senior Clinical Research Laboratory Manager for UPMC Clinical Research Services with over 15 years of experience in laboratory science, and over 10 years’ experience in GMP, GCLP, and Clinical Research Laboratory science. She oversees over 300 clinical trial protocols’ correlatives and ensures staff are adequately trained in correlative sample collection and processing to allow clinical trial protocols to meet their objectives. Jamie is the mom of two highly energetic young boys and one not-so-energetic cat.