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PDA Journal of Pharmaceutical Science and Technology|April 10, 2013
Identification of a leachable compound detrimental to cell growth in single-use bioprocess containersMatthew Hammond, Heather Nunn, Gary Rogers, et al.PDA Journal of Pharmaceutical Science and Technology|June 12, 2013
Formulation, development, and evaluation of floating pulsatile drug delivery system of atenololSwati C Jagdale, Monali S Sali, Ajay L Barhate, et al.PDA Journal of Pharmaceutical Science and Technology|October 3, 2013
Perspectives on the PQRI Extractables and Leachables "Safety Thresholds and Best Practices" Recommendations for Inhalation Drug ProductsDaniel L Norwood, Lee M Nagao, Cheryl L M StultsPDA Journal of Pharmaceutical Science and Technology|November 28, 2012
The reliability-quality relationship for quality systems and quality risk managementH Gregg Claycamp, Faiad Rahaman, Jason M UrbanPDA Journal of Pharmaceutical Science and Technology|November 28, 2012
Information Processing: Rate-Based Investigation of Cell Physiological Changes along Design Space DevelopmentPatrick Sagmeister, Patrick Wechselberger, Christoph HerwigPDA Journal of Pharmaceutical Science and Technology|November 28, 2012
Routine screening for the presence of adulteration in raw materials using automated nuclear magnetic resonance spectroscopyDavid Meriage, Gary Rogers, Joseph PhillipsPDA Journal of Pharmaceutical Science and Technology|November 28, 2012
Application of quality risk management to set viable environmental monitoring frequencies in biotechnology processing and support areasTim SandlePDA Journal of Pharmaceutical Science and Technology|November 28, 2012
Case Study: A Novel Bacterial Contamination in Cell Culture Production--Leptospira licerasiaeJoseph Chen, Jesse Bergevin, Robert Kiss, et al.PDA Journal of Pharmaceutical Science and Technology|June 1, 2026
In-situ Verification of Disinfection Rotation for Contamination ControlLaura Brennan, Dr Terra Kremer, Gary Feehan, et al.PDA Journal of Pharmaceutical Science and Technology|June 1, 2026
Single-Use Systems between Compliance and Circularity: A Critical View under EU-GMP-Annex 1 and European Green DealNicolas HuberPageof 136