Cell & Gene Therapy
Access new resources for advanced therapy development, from candidate identification through market authorization.
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Harness the power to transform clinical development
Reimagine clinical development by intelligently connecting data, technology, and analytics to optimize your trials. The result? Faster decision making and reduced risk so you can deliver life-changing therapies faster.
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Generate and disseminate evidence that answers crucial clinical, regulatory and commercial questions, enabling you to drive smarter decisions and meet your stakeholder needs with confidence.
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Orchestrate your success across the complete compliance lifecycle with best-in-class services and solutions for safety, regulatory, quality and medical information.
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When your destination is a healthier world, making intelligent connections between data, technology, and services is your roadmap.
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WHITE PAPER
Decisions in Cell and Gene Therapy Development
Implications across the development landscape
Apr 12, 2024
This white paper delves into the key decisions required in the development of cell and gene therapies and explores their profound impact on subsequent stages of the therapy’s life cycle. From early decisions on indication prioritization, engagement with patients and patient advocacy groups, manufacturing and contract development and manufacturing organization (CDMO) selection, to long term follow up design, each decision bears consequences that ripple across regulatory approval, commercial viability, market access, and further iterations of therapy development. By mapping these decisions at the earliest possible point, stakeholders can navigate the complex landscape of cell and gene therapy development with enhanced precision and insight.
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Specialized expertise and customized solutions across 14 therapeutic centers of excellence, including oncology, GI/NASH, pediatrics, neurology and rare diseases.