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Journal of Quality Technology
A Quarterly Journal of Methods, Applications and Related Topics
Volume 12, 1980 - Issue 3
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Reviews of Standards and Specifications

Evaluation of U. S. Pharmacopeia Sampling Plans for Dissolution

Charles B. PheattG. D. Searle & Co., Research and Development Division, Skokie, Illinois60680View further author information
Pages 158-164 | Published online: 22 Feb 2018

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Read on this site (2)

Yi Tsong, Meiyu Shen & Vinod P. Shah. (2004) Three-Stage Sequential Statistical Dissolution Testing Rules. Journal of Biopharmaceutical Statistics 14:3, pages 757-779.
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Yi Tsong, Thomas Hammerstrom, Karl Lin & Ting Eng Ong. (1995) Dissolution test acceptance sampling plans . Journal of Biopharmaceutical Statistics 5:2, pages 171-183.
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Articles from other publishers (3)

K. Govindaraju & R. Kissling. (2014) A combined attributes–variables plan. Applied Stochastic Models in Business and Industry 31:5, pages 575-583.
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Tom Gravestock, Karl Box, John Comer, Elizabeth Frake, Sam Judge & Rebeca Ruiz. (2011) The “GI dissolution” method: a low volume, in vitro apparatus for assessing the dissolution/precipitation behaviour of an active pharmaceutical ingredient under biorelevant conditions. Analytical Methods 3:3, pages 560.
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Siobhán Hayes, Adrian Dunne, Trevor Smart & John Davis. (2004) Interpretation and Optimization of the Dissolution Specifications for a Modified Release Product with an In Vivo–In Vitro Correlation (IVIVC). Journal of Pharmaceutical Sciences 93:3, pages 571-581.
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