Reducing The Risk During Cell And Gene Therapy Development And Manufacturing

Overview


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While new modalities are generating significant excitement among patients and caregivers, cell and gene therapy manufacturers are experiencing growing pains. The rapid growth and continued momentum of the industry has led to the issuance of new guidance. In this article we share insights for navigating within a novel and complex regulatory environment, mitigating risks posed by raw materials and implementing proper risk assessments during manufacturing.

This content is provided by MilliporeSigma - Gene Therapy, and any views and opinions expressed do not necessarily reflect those of Biopharma-Reporter.com

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CDMO Process Development Template

CDMO Process Development Template

Content provided by MilliporeSigma - Gene Therapy

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Process development is a crucial step in viral vector manufacturing and a successful CDMO partnership can help navigate the challenges associated with scaling your viral vector.

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