Innovative in vitro methodologies for establishing therapeutic equivalence
ABSTRACT To improve the quality of pharmaceutical products in their markets, several Latin American countries have begun to require that new generic products demonstrate bioequivalence against innovator or reference products. However, given the number of products involved, it is not feasible to rely...
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| Main Authors: | , , , , |
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| Format: | Book |
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Pan American Health Organization.
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Internet
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A1234.567 |
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| Copy 1 | Available |