Statistical comparison of dissolution profiles
Author:
Affiliation:
1. Department of Chemical and Biochemical Engineering, Rutgers University, Piscataway, NJ, USA and
2. Snee Associates, LLC, Newark, DE, USA
Publisher
Informa UK Limited
Subject
Organic Chemistry,Drug Discovery,Pharmaceutical Science,Pharmacology
Link
https://www.tandfonline.com/doi/pdf/10.3109/03639045.2015.1078349
Reference44 articles.
1. FDA. Guidance for Industry: Modified Release Solid Oral Dosage Forms: Scale-up and Post Approval Changes (SUPAC-MR): Chemistry, Manufacturing and Controls; In Vitro Dissolution Testing and In Vivo Bioequivalence Documentation. 1997
2. FDA. Guidance for Industry: Extended Release Oral Dosage Forms- Development, Evaluation, and Application of In Vitro/In Vivo Correlations. 1997
3. FDA. Guidance for Industry: Dissolution Testing of Immediate Release Solid Oral Dosage Forms. 1997
4. Comparison of in vitro dissolution profiles by ANOVA-based, model-dependent and -independent methods
5. A Novel Bending Point Criterion for Dissolution Profile Interpretation
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