Manufacturing

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Tolerance Interval Approach for the Determination of Overfill of Liquid Parenteral Drug Products
Bernhard Schmelzer and Marc Sutter

PDA Journal of Pharmaceutical Science and Technology May 2023, 77 (3) 181-196; DOI: https://doi.org/10.5731/pdajpst.2022.012743
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Enhancement of Cell-Based Vaccine Manufacturing through Process Intensification
William Whitford, Alain M. SourabiÈ and Dushyant B. Varshney

PDA Journal of Pharmaceutical Science and Technology March 2022, 76 (2) 151-162; DOI: https://doi.org/10.5731/pdajpst.2020.012583
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Overview of “The Study in Risk-Based Manufacturing Environmental Control for Non-Sterile Drug Products”
Osamu Shirokizawa, Keisuke Inoue and Tsutomu Kamikukita

PDA Journal of Pharmaceutical Science and Technology November 2021, 75 (6) 490-505; DOI: https://doi.org/10.5731/pdajpst.2018.009308
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Proceedings of the 2017 Viral Clearance Symposium Session 5: Facility Risk Mitigation
Junfen Ma and Thomas R. Kreil

PDA Journal of Pharmaceutical Science and Technology September 2018, 72 (5) 511-515; DOI: https://doi.org/10.5731/pdajpst.2018.009175

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