Webinar 3-1

Do You Even Science?

Big Picture Challenges of Protocol Compliance and Back to Basics Innovation on the Fundamentals of Clinical Research

 

Watch this enlightening webinar where industry leaders converged to unveil the pivotal role of protocol compliance in clinical research success.
🎯 Learning Objectives:
  • 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.

  • Gain insights into innovative strategies and next-generation approaches to enhance protocol adherence and mitigate costly disruptions.

Learn how optimizing compliance can streamline data management, biostatistics, and regulatory strategies, ultimately boosting overall drug development efficiency.

Slick Playground

Deepi-1

Deepi Minhas

Quality Capability and Risk Manager, GSK

Patrick-1

Patrick Zbyszewski

Sr. Director Data Management, Loxo Oncology

Tamei-1

Tamei Elliott

Assoc. Director, Scientific Programs, DIA

Lauren briggs-1

Lauren Briggs

SVP of Customer Success, ProofPilot

Rick Ward

Rick Ward

SVP, US Business Development, CluePoints

Joseph Kim-1

Joseph Kim

Chief Strategy Officer, ProofPilot

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