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Published in 2021 at "Advanced drug delivery reviews"
DOI: 10.1016/j.addr.2021.113895
Abstract: Many pharmaceutical developers of generic orally inhaled products (OIPs) are facing significant issues in passing the regulatory requirement to show pharmacokinetic (PK) bioequivalence (BE) to the originator product. The core of the issue is that…
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Keywords:
bioequivalence;
products ivivc;
aerosol products;
assessment pharmaceutical ... See more keywords