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Published in 2024 at "Pharmaceutics"
DOI: 10.3390/pharmaceutics16121579
Abstract: Background: When companies are uncertain about the potential of a new formulation to be bioequivalent to a Reference product, it is common practice to carry out downsized pilot studies as a gatekeeping in vivo strategy…
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Keywords:
methodology;
cmax factor;
pilot;
bioequivalence ... See more keywords