Do You Even Science?
Big Picture Challenges of Protocol Compliance and Back to Basics Innovation on the Fundamentals of Clinical Research
Date: Feb 28 | 11 AM EST
Join us for an enlightening webinar where industry leaders converge to unveil the pivotal role of protocol compliance in clinical research success.
🎯 Learning Objectives:
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Explore the critical downstream effects of protocol non-compliance on research outcomes, operations, and regulatory approvals.
Understand how poor data quality resulting from non-compliance can disrupt downstream processes and jeopardize drug development viability.
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Gain insights into innovative strategies and next-generation approaches to enhance protocol adherence and mitigate costly disruptions.
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Learn how optimizing compliance can streamline data management, biostatistics, and regulatory strategies, ultimately boosting overall drug development efficiency.
Discover the broader implications for drug development divisions and the strategic imperative of securing regulatory approvals.
Register now for an unmissable event that promises actionable insights and invaluable networking opportunities.
Deepi Minhas
Quality Capability and Risk Manager, GSK
Patrick Zbyszewski
Sr. Director Data Management, Loxo Oncology
Tamei Elliott
Assoc. Director, Scientific Programs, DIA
Lauren Briggs
SVP of Customer Success, ProofPilot
Rick Ward
SVP, US Business Development, CluePoints
Joseph Kim
Chief Strategy Officer, ProofPilot