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The AAPS Journal|May 21, 2021
Systems Modeling to Quantify Safety Risks in Early Drug Development: Using Bifurcation Analysis and Agent-Based Modeling as ExamplesCarmen Pin, Teresa Collins, Megan Gibbs, et al.
The AAPS Journal|August 7, 2016
A Quantitative Review and Meta-Models of the Variability and Factors Affecting Oral Drug Absorption-Part I: Gastrointestinal pHAhmad Y Abuhelwa, David J R Foster, Richard N Upton
The AAPS Journal|August 29, 2009
Evaluation of an extended grid method for estimation using nonparametric distributionsRadojka M Savic, Mats O Karlsson
The AAPS Journal|July 25, 2012
Bioequivalence requirements in the European Union: critical discussionAlfredo García-Arieta, John Gordon
The AAPS Journal|September 3, 2013
Flow imaging microscopy for protein particle analysis--a comparative evaluation of four different analytical instrumentsSarah Zölls, Daniel Weinbuch, Michael Wiggenhorn, et al.
The AAPS Journal|August 3, 2016
Nanomedicines: From Bench to Bedside and BeyondHenry Havel, Gregory Finch, Pamela Strode, et al.
The AAPS Journal|January 20, 2007
Endocannabinoid metabolomics: a novel liquid chromatography-mass spectrometry reagent for fatty acid analysisJohn Williams, Lakshmipathi Pandarinathan, JodiAnne Wood, et al.
The AAPS Journal|July 1, 2026
In vivo Predictive Dissolution Test Using Biorelevant Bicarbonate Buffer for High-dose Free Acid DrugYuki Tarumi, Kiyohiko Sugano
The AAPS Journal|July 28, 2026
Assessment of Sorbitol as a Pharmaceutical Excipient in Oral Liquid Pediatric Formulations Submitted to the U.S. FDAGelareh A Abulwerdi, Brianna Cote, Susan Abdel-Rahman, et al.
The AAPS Journal|July 7, 2007
Best practices during bioanalytical method validation for the characterization of assay reagents and the evaluation of analyte stability in assay standards, quality controls, and study samplesWilliam Nowatzke, Eric Woolf
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