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Model-Based Bioequivalence assessment of a commercial Azithromycin Capsule against Pfizer Zithromax® Tablet marketed in Jamaica
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Study of regulatory requirements for the conduct of bioequivalence studies in US, Europe, Canada, India, ASEAN and SADC countries: Impact on generic drug substitution
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DOI: 10.7324/JAPS.2016.60430Pages: 206-222
Model integrated evidence approach for rational and safe formulation development: case of alfuzosin prolonged-release tablets
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