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For complex generics including products with modified-release mechanisms, topical delivery systems, or inhalation devices demonstrating bioequivalence requires additional in vitro testing and sometimes in vivo pharmacodynamic studies, adding development time and cost
Friedman test was employed to determine the changes in the mean of the outcome variables at baseline, week 5, and week 10
The Journal of Reproductive Medicine
Off-patent players may need to develop distinct, memorable branding strategies that support these activities
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