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February 2, 2026PDA Journal of Pharmaceutical Science and Technology0 citations

A QbD Framework for Efficient Technology Transfer in Biologics Manufacturing

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DODogan Ornek

Key Points

  • The aim is to present a Quality by Design (QbD) framework to enhance technology transfer in biologics manufacturing.
  • Implementation of QbD principles across five key stages: Scope of Work Development, Information Transfer, Tech Transfer and Pilot Runs, Pre-Production Activities, and cGMP Production.
  • Systematic framework outlines strategies for effective technology transfer and resource utilization.
  • Improved technology transfer efficiency through the adoption of QbD principles.
  • Enhanced scalability and reproducibility of processes in biologics manufacturing.
  • Consistent product quality maintained in alignment with regulatory standards.

Abstract

Technology transfer from clients to contract development and manufacturing organizations is a complicated process and inclusion of scale-up and scale-down strategies brings additional complexity. These complexities can lead to extended development timelines and significant resource utilizations to meet regulatory compliance. This manuscript presents the implementation of Quality by Design (QbD) principles as a systematic framework to mitigate these challenges and improve technology transfer efficiency. Here I provide a strategic approach to integrate QbD across five key stages of technology transfer: Scope of Work Development, Information Transfer and Failure Mode and Effects Analysis, Technology Transfer and Pilot Runs, Pre-Production Activities, and cGMP Production. By adopting this QbD-driven methodology, companies can achieve more effective knowledge transfer, develop scalable and reproducible processes, and ensure consistent product quality in alignment with regulatory standards.

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Cite This Study

Dogan Ornek (2026) studied this question.

synapsesocial.com/papers/6980fe68c1c9540dea8107efhttps://doi.org/10.5731/pdajpst.2025-000074.1
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