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W2088473012 abstract "Currently, the EMEA, FDA, and WHO as regulatory authorities accept rapidly dissolving (>85% dissolved in 30 min) biopharmaceutics classification system (BCS) I drug products for biowaiver candidates. In the draft EMEA guideline the requirement has been set tighter, that is, the drug product should be very rapidly dissolving (>85% dissolved in 15 min) to be eligible for a biowaiver. Pharmacokinetic modeling of 32 BCS I drugs was performed to demonstrate that very rapid dissolution is not necessary to guarantee bioequivalence for them. Rapid dissolution and similar dissolution profiles are sufficient criteria for all BCS I drugs. © 2009 Wiley-Liss, Inc. and the American Pharmacists Association J Pharm Sci 99:621–625, 2010" @default.
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W2088473012 date "2010-02-01" @default.
W2088473012 modified "2023-10-17" @default.
W2088473012 title "Very rapid dissolution is not needed to guarantee bioequivalence for biopharmaceutics classification system (BCS) I drugs" @default.
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W2088473012 doi "https://doi.org/10.1002/jps.21879" @default.
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