Author:
Krishna Rajesh,Luo Wen-Lin,Larson Patrick J.,Fackler Paul H.
Reference6 articles.
1. Sequential design approaches for bioequivalence studies with crossover designs;Potvin;Pharm Stat,2007
2. Non-traditional study designs to demonstrate average bioequivalence for highly variable drug products;Patterson;Eur J Clin Pharmacol,2001
3. An extension of Bayesian expected power and its application in decision making;Liu;J Biopharm Stat,2010
4. Guidance for Industry: Conduct and Analysis of Bioavailability and Bioequivalence Studies–Part A: Oral Dosage Formulations Used for Systemic Effects,1992
5. Guideline for Bioequivalence Studies of Generic Products,2012
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