How Veeva LIMS Is Helping Forge Biologics Scale QC For Rapid Growth

Rapid growth in cell and gene therapy manufacturing has pushed CDMOs to modernize quality control processes. Forge Biologics transitioned from paper-based documentation to Veeva LIMS, creating a streamlined, scalable approach for QC operations. This shift reduces documentation errors, accelerates method execution, and automates time-intensive tasks like generating certificates of analysis and stability reports. By integrating QC data with quality systems, Forge gains real-time visibility, improves compliance, and enhances client access to critical insights. The result is a more efficient workflow that saves hours per batch and supports GMP readiness for late-stage and commercial programs.

Learn how Forge leveraged cloud-based solutions to optimize QC processes and deliver greater value to clients.