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Aug 2, 2008
By:
Karen A. Russo, Roger L. Williams
Pharmaceutical Technology
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USP's guideline for pending monographs can speed up publication of monograhs and time to market.  Mar 2, 2008
By:
Thomas S. Foster, Darrell R. Abernathy, William F. Koch, Walter W. Hauck, PhD
Pharmaceutical Technology
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The United States Pharmacopeia emphasizes mechanical calibration and a performance test to esnure integrity of the dissolution procedure. Nov 2, 2007
By:
Roger L. Williams, Darrell R. Abernethy
Pharmaceutical Technology
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Representatives from 17 nations sit down to decide upon standards-setting initiatives. Aug 2, 2007
By:
Roger L. Williams, Todd L. Cecil, Ruth K. Miller, Stefan Schuber, PhD
Pharmaceutical Technology
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USP is revising key documents to make them easier to use. May 2, 2007
By:
Ronald G. Manning, PhD, Samir Z. Wahab, PhD, William E. Brown, Walter W. Hauck, PhD, Stefan Schuber, PhD, Roger L. Williams
Pharmaceutical Technology
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USP applies metrological principles to the dissolution procedure alone and in collaborative studies to understand and minimize potential sources of variability. Oct 2, 2006
By:
Todd L. Cecil, Roger L. Williams
Pharmaceutical Technology
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Efforts to solicit new monographs have fallen behind the rate of NDA approvals, while analytical techniques have become outdated because of advances in analytical technologies.
Mar 2, 2006
By:
Horacio Pappa, PhD, David Porter, PhD, Karen Russo, PhD
Pharmaceutical Technology
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USP's proposed General Chapter 1226 "Verification of Compendial Procedures" aims to provide guidance about the verification process. Nov 2, 2005
By:
Kahkashan Zaidi, Paul D. Curry, Jr., Shawn C. Becker
Pharmaceutical Technology
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USP monographs, if they are consistently observed and applied, can help reduce medical gas errors. Apr 2, 2005
By:
Roger L. Williams, MD
Pharmaceutical Technology
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At its 2005 Convention, USP passed 13 resolutions that will help define the organizations path for the next five years and represent the interests of its diverse constituency.
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