1. Immediate Release Solid Oral Dosage Forms, Scale-Up and Postapproval Changes: Chemistry, Manufacturing, and Controls, in Vitro Dissolution Testing, and in Vivo Bioequivalence Documentation;Guidance for Industry,1995
2. For Bioequivalence Studies of Generic Products (Revision);Guideline,2012
3. For Bioequivalence Studies of Generic Products for Different Strengths of Oral Solid Dosage Forms (Revision);Guideline,2012
4. On the Investigation of Bioequivalence;Guideline,2010
5. International guidelines for bioequivalence of systemically available orally administered generic drug products: a survey of similarities and differences;Davit;AAPS J.,2013