1. Analysis of drug dissolution data
2. Food and Drug Administration. FDA Guidance for Industry: Immediate Release Solid Dosage Forms: Scale-up and Post-Approval Changes (SUPAC-IR): Chemistry, Manufacturing and Controls. In Vitro Dissolution Testing and In Vivo Bioequivalence Documentation; FDA November 1995
3. Food and Drug Administration. FDA Guidance for Industry: Dissolution Testing of Immediate Release Solid Oral Dosage Forms; FDA August 1997
4. Food and Drug Administration. FDA Guidance for Industry: Extended Release Oral Dosage Forms: Development, Evaluation and Application of In Vitro/In Vivo Correlations; FDA September 1997