Integration of quality by design with artificial intelligence/machine learning technologies in pharmaceutical manufacturing: A comprehensive review

Review paper

Authors

  • Sumit Ghosal School of Pharmacy, The Neotia University, 24 Parganas (South), West Bengal 743368, India https://orcid.org/0009-0005-3233-4237
  • Niranjan Panda School of Pharmacy, The Neotia University, 24 Parganas (South), West Bengal 743368, India https://orcid.org/0000-0002-1821-7326
  • Bikash Ranjan Jena School of Pharmacy, The Neotia University, 24 Parganas (South), West Bengal 743368, India https://orcid.org/0000-0001-9722-4454
  • Madhusudan Maity School of Pharmacy, The Neotia University, 24 Parganas (South), West Bengal 743368, India https://orcid.org/0009-0006-8996-4798
  • Sankhadip Bose School of Pharmacy, The Neotia University, 24 Parganas (South), West Bengal 743368, India https://orcid.org/0000-0001-7327-1619
  • Rabinarayan Parhi Department of Pharmaceutical Sciences, Sushruta School of Medical and Paramedical Sciences, Assam University (A Central University), Silchar 788011, Assam, India https://orcid.org/0000-0003-4010-4368

DOI:

https://doi.org/10.5599/admet.3565

Keywords:

Quality by testing, critical quality attributes, deep neural networks, process analytical technology, digital twins, continuous manufacturing

Abstract

Background and purpose: Quality by design (QbD) has revolutionized pharmaceutical development by shifting from a conventional quality-by-testing approach to a science-based approach that incorporates quality into products and processes from inception. The integration of artificial intelligence (AI), machine learning (ML), automation, and digital technologies with QbD offers new opportunities to enhance process understanding, optimize critical quality attributes (CQAs) and support the Pharma 4.0 industry framework. Experimental approach: A systematic review of studies published between 2016 and 2025 was conducted to evaluate the application of supervised learning algorithms, deep neural networks, reinforcement learning, and digital twin technologies within QbD. Regulatory frameworks, including International Council for Harmonisation (ICH) quality guideline Q8 through Q14, the U.S. Food and Drug Administration’s Emerging Technology Program and the European Medicines Agency quality initiative, together with representative industrial case studies, were also examined. Key results: This review demonstrates that AI-driven QbD improves process understanding, CQA optimization, batch-to-batch consistency, process robustness, and real-time quality control. Further, advanced computational models enable predictive process monitoring, intelligent decision-making, and in silico experimentation, reducing manufacturing costs, development time and experimental burden. However, challenges related to data quality, model interpretability, validation, and regulatory harmonisation remain a critical barrier to widespread implementation. Conclusion: The convergence of AI, ML and QbD provides a robust framework for intelligent pharmaceutical manufacturing (PM). AI-enabled QbD supports the development of high-quality products through predictive, data-driven, and in silico approaches while accelerating development and improving manufacturing efficiency. These technologies offer a practical roadmap toward Pharma 4.0 and the future of digital PM.

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03-09-2026

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Integration of quality by design with artificial intelligence/machine learning technologies in pharmaceutical manufacturing: A comprehensive review: Review paper. (2026). ADMET and DMPK, 14, Article 3565. https://doi.org/10.5599/admet.3565

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