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The American Association of Pharmaceutical Scientists
Commentary
James Blanchard, James Coleman, Courtney Crim, Claire D’Abreu-Hayling, Lou Fries, Raouf Ghaderi, Barbara Haeberlin, Richard Malcolmson, Stanley Mittelman and Lee Nagao, et al.
Journal Article
Foreign Particles Testing in Orally Inhaled and Nasal Drug Products
James Blanchard, James Coleman, Claire D’Abreu Hayling, Raouf Ghaderi and Barbara Haeberlin, et al.
Pharmaceutical Research, 2004, Volume 21, Number 12, Pages 2137-2147
Book Chapter
Combination Products/Drugs in Devices
Jon V. Beaman and Roisin Wallace
2009, Handbook of Stability Testing in Pharmaceutical Development, Part III, Pages 323-351
Best Practices for Extractables and Leachables in Orally Inhaled and Nasal Drug Products: An Overview of the PQRI Recommendations
Daniel L. Norwood, Diane Paskiet, Michael Ruberto, Thomas Feinberg and Alan Schroeder, et al.
Pharmaceutical Research, 2008, Volume 25, Number 4, Pages 727-739
Pharmaceutical Quality by Design: Product and Process Development, Understanding, and Control
Lawrence X. Yu
Pharmaceutical Research, 2008, Volume 25, Number 4, Pages 781-791
Genetics and intelligence: new approaches in production engineering
Berend Denkena, Helge Henning and Leif-Erik Lorenzen
Production Engineering, 2010, Volume 4, Number 1, Pages 65-73
An Aircraft Accident Investigation: Revisited
S. K. Bhaumik
Journal of Failure Analysis and Prevention, 2008, Volume 8, Number 5, Pages 399-405
Quality by Design: Concepts for ANDAs
Robert A. Lionberger, Sau Lawrence Lee, LaiMing Lee, Andre Raw and Lawrence X. Yu
The AAPS Journal, 2008, Volume 10, Number 2, Pages 268-276
Content Uniformity and Dose Uniformity: Current Approaches, Statistical Analyses, and Presentation of an Alternative Approach, with Special Reference to Oral Inhalation and Nasal Drug Products
Roger L. Williams, Wallace P. Adams, Guirag Poochikian and Walter W. Hauck
Pharmaceutical Research, 2002, Volume 19, Number 4, Pages 359-366
Commentary on AAPS Workshop Dissolution Testing for the Twenty-first Century: Linking Critical Quality Attributes and Critical Process Parameters to Clinically Relevant Dissolution
Cheng Tong, Susan S. D’Souza, Jan E. Parker and Tahseen Mirza
Pharmaceutical Research, 2007, Volume 24, Number 9, Pages 1603-1607
Reference Work Entry
Glass: Theory of crystallization
David Duke
Encyclopedia of Earth Sciences Series, 1981, Mineralogy, Pages 189-191
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