1. US Food and Drug Administration, Rockville, MD, USA (1997) Guidance for Industry, Dissolution Testing of Immediate Release Solid Oral Dosage Forms
2. US Food and Drug Administration, Rockville, MD, USA (1995) Guidance for Industry, Immediate Release Solid Oral Dosage Forms, Scale-up and Post-approval Changes: Chemistry, Manufacturing and Controls, In Vitro Dissolution Testing, and In Vivo Bioequivalence Documentation
3. US Food and Drug Administration, Rockville, MD, USA (1997) Guidance for Industry, SUPAC–MR Modified Release Solid Oral Dosage Forms, Scale-up and Post-approval Changes: Chemistry, Manufacturing and Controls, In Vitro Dissolution Testing, and In Vivo Bioequivalence Documentation
4. US Food and Drug Administration, Rockville, MD, USA (1997) Guidance for Industry, Extended Release Solid Oral Dosage Forms, Development, Evaluation and Application of In Vitro/In Vivo Correlations