IQVIA BIOTECH

Unlock smarter clinical trial design

DOWNLOAD WHITE PAPER: Accelerate Drug Development with Master Protocols

As clinical trial complexity increases, the need for faster, more adaptive approaches to drug development is clear. The pharmaceutical industry is embracing master protocols to accelerate timelines, streamline operations and optimize patient access.

By leveraging flexible trial designs — such as basket, umbrella, and platform trials — sponsors can evaluate multiple therapies or indications under a single protocol, reducing duplication and accelerating insights.

In this white paper, we explore how working with a CRO in adaptive design and operational execution can help sponsors navigate complexity and bring effective therapies to patients, faster.

Meet the Authors

Design, execute and optimize master protocol trials that accelerate development timelines and regulatory decisions. From complexity to clarity, we’ve got you.

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We listen, you succeed, lives improve. Let us know how we can support your clinical development program, bring your innovation to market and maximize patient impact.

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Beth Chamblin

Senior Director, Project Management, Oncology

IQVIA Biotech

Kelley Coalier, MS, MBA

Associate Principal, Enterprise Transformation Strategy

IQVIA

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