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PDA Journal of Pharmaceutical Science and Technology|February 16, 2017
Validation of Milliflex® Quantum for Bioburden Testing of Pharmaceutical ProductsOliver Gordon, Marcel Goverde, Alexandra Staerk, et al.
PDA Journal of Pharmaceutical Science and Technology|August 18, 2019
Points to Consider: Best Practices to Identify Particle Entry Routes along the Manufacturing Process for Parenteral FormulationsSylvia Anger, Cecile Begat, Vincent Crnko, et al.
PDA Journal of Pharmaceutical Science and Technology|August 18, 2019
Quantifying the Vial-Capping Process: Reexamination Using Micro-Computed TomographyRobert Ovadia, Philippe Lam, Vassia Tegoulia, et al.
PDA Journal of Pharmaceutical Science and Technology|August 18, 2019
Long-Term Study of Container Closure Integrity of Rubber-Glass Vial Systems by Multiple MethodsMatthew R Gehrmann, T Page Mcandrew
PDA Journal of Pharmaceutical Science and Technology|March 27, 2014
Use of a real-time microbial air sampler for operational cleanroom monitoringT Eaton, C Wardle, W Whyte
PDA Journal of Pharmaceutical Science and Technology|March 27, 2014
FDA 2011 process validation guidance: lifecycle compliance modelCliff Campbell
PDA Journal of Pharmaceutical Science and Technology|December 1, 2007
Preparation and physicochemical and preclinical evaluations of recrystallized celecoxibS Mutalik, N Usha, A K Ranjith, et al.
PDA Journal of Pharmaceutical Science and Technology|December 1, 2007
Evolution of endotoxin contamination during production of a therapeutic serumHugo Massaldi, Victor Morais
PDA Journal of Pharmaceutical Science and Technology|December 1, 2007
In vivo and in vitro evaluation of a solid dispersion system of gliclazide:PEG 6000Sukmadjaja Asyarie, Heni Rachmawati
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