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PDA Journal of Pharmaceutical Science and Technology|December 16, 2025
The European Qualified Person: Legal Accountability, Quality Leadership, and AI Integration in Modern Pharmaceutical ManufacturingMario StassenPDA Journal of Pharmaceutical Science and Technology|April 18, 2026
Beyond Batch Release: Responsible Decision-Making, Professional Judgement, and Governance in Complex Pharmaceutical ManufacturingMario StassenReproductive Biomedicine Online|September 16, 2014
Safety aspects and side-effects of ExEm-gel and foam for uterine cavity distension and tubal patency testingNiek Exalto, Mario Stassen, Mark Hans EmanuelPDA Journal of Pharmaceutical Science and Technology|July 31, 2026
From Traditional Statistics to Adaptive Multivariate Models: Exploring the Role of AI in Modern Pharmaceutical ManufacturingMario Stassen, Matt Schmucki, Francisco Valero, et al.PDA Journal of Pharmaceutical Science and Technology|February 16, 2026
Bridging Guidance and Regulation: Interpreting the Draft Annex 22 on Artificial Intelligence in GMP ManufacturingMario Stassen, Matt Schmucki, Fransisco Barranco, et al.PDA Journal of Pharmaceutical Science and Technology|December 27, 2024
Recommendations for Artificial Intelligence Application in Continued Process Verification: A Journey Toward the Challenges and Benefits of AI in the Biopharmaceutical IndustryMario Stassen, Catarina S Leitão, Toni Manzano, et al.Pageof 1